Compositions and methods related to excipients and cannabinoid formulations

ABSTRACT

Various aspects of this patent document relate to beverage concentrates that comprise active ingredients, containers comprising beverage concentrates, and methods to prepare beverage formulations from beverage concentrates.

CROSS-REFERENCE TO RELATED APPLICATIONS

This patent application claims priority to U.S. Provisional Patent Application No. 63/059,829, filed Jul. 31, 2020; U.S. Provisional Patent Application No. 63/130,560, filed Dec. 24, 2020; U.S. Provisional Patent Application No. 63/148,047, filed Feb. 10, 2021; U.S. Provisional Patent Application No. 63/154,480, filed Feb. 26, 2021; U.S. Provisional Patent Application No. 63/154,507, filed Feb. 26, 2021; U.S. Provisional Patent Application No. 63/154,538, filed Feb. 26, 2021; U.S. Provisional Patent Application No. 63/154,579, filed Feb. 26, 2021; U.S. Provisional Patent Application No. 63/191,814, filed May 21, 2021; U.S. Provisional Patent Application No. 63/191,830, filed May 21, 2021; U.S. Provisional Patent Application No. 63/191,844, filed May 21, 2021; U.S. Provisional Patent Application No. 63/191,872, filed May 21, 2021; U.S. Provisional Patent Application No. 63/194,810, filed May 28, 2021; U.S. Provisional Patent Application No. 63/228,563, filed Aug. 2, 2021; U.S. Provisional Patent Application No. 63/228,572, filed Aug. 2, 2021; and U.S. Provisional Patent Application No. 63/228,594, filed Aug. 2, 2021, each of which is incorporated by reference in its entirety.

BACKGROUND

Improved formulations to administer hydrophobic active agents are desirable.

BRIEF DESCRIPTION

Various aspects of this disclosure relate to the discovery that hydrophobic active ingredients can be dissolved in propylene glycol and combined with a carbohydrate to produce a powder that is wetted by the propylene glycol, and that such powders are effective at dispersing hydrophobic active ingredients in beverages. Without limiting this disclosure or any patent claim that matures from this patent document, the propylene glycol and carbohydrate allow for the separation of hydrophobic active ingredients over a broad surface area, and the propylene glycol and carbohydrate can be dissolved in beverages rapidly enough to disperse the hydrophobic active ingredients in the beverage while minimizing the propensity of the hydrophobic active ingredients to recombine into a lipid phase.

DETAILED DESCRIPTION

Various aspects of this disclosure relate to a composition, comprising a solid phase and a liquid phase, wherein the solid phase has a surface-area-to-volume ratio that is greater than 500 per meter; the solid phase consists of ingredients; the ingredients of the solid phase comprise carbohydrates; the carbohydrates comprise one or more of alginic acid, alginate, propylene glycol alginate, inulin, arabinogalactan, lignosulfonate, carrageenan, furcelleran, pullulan, glucomannan, gellan gum, gum arabic, gellan gum, gum ghatti, guar gum, gum karaya, tara gum, tragacanth, xanthan gum, carboxymethylcellulose, hydroxyethyl cellulose, ethylhydroxyethylcellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, modified starch, dextrin, polydextrose, pectin, beta-glucan, lactobionic acid, lactobionate, isomalt, erythritol, threitol, arabitol, xylitol, ribitol, mannitol, sorbitol, galactitol, fucitol, iditol, inositol, volemitol, sucrose, lactose, maltose, trehalose, maltitol, glucose, fructose, galactose, arabinose, ribose, xylose, allulose, sorbose, tagatose, fucose, mannose, and hydrogenated starch hydrolysate; at least 90 percent of the ingredients of the solid phase consist of the carbohydrates by mass; the composition comprises the liquid phase at a concentration of at least 0.5 percent and no greater than 15 percent by mass; the composition comprises the solid phase at a concentration of at least 85 percent and no greater than 99.5 percent by mass; the composition comprises at least 2 and no greater than 4 calories of food energy per gram of the composition; the liquid phase comprises a concentration of calories of food energy per gram of the liquid phase; the solid phase comprises a concentration of calories of food energy per gram of the solid phase that is less than the concentration of calories of food energy per gram of the liquid phase; the liquid phase consists of ingredients that comprise a solvent; each of the ingredients of the liquid phase has a concentration by mass in the liquid phase; the concentration by mass of the solvent in the liquid phase is greater than the concentration by mass of any of the other ingredients of the liquid phase; and the solvent is propane-1,2-diol.

“Comprise” refers to an open set such that ingredients that comprise a solvent can also comprise, for example, and active ingredient.

“Food calorie” refers to a North American food calorie, which is equal to a European Union food kilocalorie, and which are both equal to 4.184 kilojoules of food energy.

Various aspects of this disclosure relate to a container that contains at least 100 milligrams and no greater than 5 grams of a composition, wherein the composition comprises a solid phase and a liquid phase; the solid phase has a surface-area-to-volume ratio that is greater than 500 per meter; the solid phase consists of ingredients; the ingredients of the solid phase comprise carbohydrates; the carbohydrates comprise one or more sugar alcohols; at least 90 percent of the ingredients of the solid phase consist of the carbohydrates by mass; the composition comprises the liquid phase at a concentration of at least 0.5 percent and no greater than 15 percent by mass; the composition comprises the solid phase at a concentration of at least 85 percent and no greater than 99.5 percent by mass; the composition comprises at least 2 and no greater than 4 calories of food energy per gram of the composition; the liquid phase comprises a concentration of calories of food energy per gram of the liquid phase; the solid phase comprises a concentration of calories of food energy per gram of the solid phase that is less than the concentration of calories of food energy per gram of the liquid phase; the liquid phase consists of ingredients that comprise a solvent; each of the ingredients of the liquid phase has a concentration by mass in the liquid phase; the concentration by mass of the solvent in the liquid phase is greater than the concentration by mass of any of the other ingredients of the liquid phase; the solvent is propane-1,2-diol; the ingredients of the liquid phase comprise an active ingredient; the active ingredient is a solute that is dissolved in the solvent of the liquid phase; the active ingredient is dissolved in the solvent of the liquid phase at a concentration of at least 200 micromolar and no greater than 250 millimolar; the active ingredient has a solubility in water at 37 degrees Celsius; the active ingredient is dissolved in the solvent of the liquid phase at a concentration that is greater than the solubility of the active ingredient in water at 37 degrees Celsius; and the active ingredient has an octanol-water partition coefficient of at least 10.

Various aspects of this disclosure relate to a method to prepare a beverage formulation, comprising providing a composition comprising an active ingredient; providing a beverage; and combining the composition with the beverage to disperse the active ingredient in the beverage and to prepare the beverage formulation, wherein the composition comprises a solid phase and a liquid phase; the solid phase has a surface-area-to-volume ratio that is greater than 500 per meter; the solid phase consists of ingredients; the ingredients of the solid phase comprise carbohydrates; at least 90 percent of the ingredients of the solid phase consist of the carbohydrates by mass; the composition comprises the liquid phase at a concentration of at least 0.5 percent and no greater than 15 percent by mass; the composition comprises the solid phase at a concentration of at least 85 percent and no greater than 99.5 percent by mass; the composition comprises at least 0.5 and no greater than 5 calories of food energy per gram of the composition; the liquid phase comprises a concentration of calories of food energy per gram of the liquid phase; the solid phase comprises a concentration of calories of food energy per gram of the solid phase that is less than the concentration of calories of food energy per gram of the liquid phase; the liquid phase consists of ingredients that comprise a solvent; each of the ingredients of the liquid phase has a concentration by mass in the liquid phase; the concentration by mass of the solvent in the liquid phase is greater than the concentration by mass of any of the other ingredients of the liquid phase; the solvent is propane-1,2-diol; the ingredients of the liquid phase comprise the active ingredient; the active ingredient is a solute that is dissolved in the solvent of the liquid phase; the active ingredient is dissolved in the solvent of the liquid phase at a concentration of at least 200 micromolar and no greater than 250 millimolar; the active ingredient has a solubility in water at 37 degrees Celsius; the active ingredient is dissolved in the solvent of the liquid phase at a concentration that is greater than the solubility of the active ingredient in water at 37 degrees Celsius; the active ingredient has an octanol-water partition coefficient of at least 10; and the beverage is a liquid that comprises water at a concentration of at least 50 molar.

In some embodiments, the composition has a color; the beverage is colorless; and the beverage formulation has a color that is different from the color of the composition.

In some embodiments, the ingredients of the liquid phase comprise a curcumin derivative selected from 5-hydroxy-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-2,4-diene-3-oxide; 5-hydroxy-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-2,5-diene-3-oxide; 5-hydroxy-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-3,5-diene-3-oxide; 5-oxo-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hept-2-ene-3-oxide; 5-oxo-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hept-3-ene-3-oxide; 2-methoxy-4-[3-hydroxy-5-oxo-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3-dienyl]phenolate; 2-methoxy-4-[5-hydroxy-3-oxo-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,4-dienyl]phenolate; 2-methoxy-4-[5-hydroxy-3-oxo-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,5-dienyl]phenolate; 2-methoxy-4-[3,5-dioxo-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hept-1-en-1-yl]phenolate; 2-methoxy-4-[3,5-dihydroxy-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3,5-trienyl]phenolate; 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3,5-triene-3-oxide; 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3,5-triene-5-oxide; 5-oxo-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3-diene-3-oxide; 3-oxo-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,4-diene-5-oxide; 3-oxo-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,5-diene-5-oxide; 2-methoxy-4-[3-hydroxy-5-oxo-7-(4-hydroxy-3-methoxyphenyl)hepta-1,3,6-trienyl]phenolate; 2-methoxy-4-[5-hydroxy-3-oxo-7-(4-hydroxy-3-methoxyphenyl)hepta-1,4,6-trienyl]phenolate; and 2-methoxy-4-[3,5-dioxo-7-(4-hydroxy-3-methoxyphenyl)hepta-1,6-dienyl]phenolate.

In some embodiments, the method comprises recording video or images of the composition both prior to and subsequent to combining the composition with the beverage.

Various aspects of this disclosure relate to a method to market a composition, comprising disseminating over the internet the video or images recorded according to a method described anywhere in this patent document.

In some embodiments, the ingredients of the liquid phase comprise one or both of 1-hydroxypropane-2-oxide and 2-hydroxypropane-1-oxide. In some specific embodiments, the liquid phase comprises propane-1,2-diol and one or both of 1-hydroxypropane-2-oxide and 2-hydroxypropane-1-oxide at a molar ratio of at least 100:1 and no greater than 1,000,000:1 (propane-1,2-diol:1-hydroxypropane-2-oxide and 2-hydroxypropane-1-oxide).

In some embodiments, the method comprises comprising combining at least 100 milligrams and no greater than 5 grams of the composition with the beverage.

In some embodiments, the composition comprises at least 10 micrograms and no greater than 100 milligrams of the active ingredient.

In some embodiments, the method comprises administering the beverage formulation to a human, wherein the human self-administers the beverage formulation by drinking it.

In some embodiments, the human presents with a health condition, and the composition comprises an amount of the active ingredient that is effective to treat the health condition.

“Treat” refers to at least one of: to cure a health condition; to increase the probability that a health condition will be cured; to shorten the time over which a health condition is cured; to increase the probability that the time necessary to cure a health condition will be shortened; to decrease the severity of a health condition; to increase the probability that the severity of a health condition will decrease; to shorten the time over which the severity of a health condition is decreased; to increase the probability that the time necessary to decrease the severity of a health condition will be shortened; to inhibit a health condition from worsening; to increase the probability that a health condition will not worsen; to delay the worsening of a health condition; to increase the probability that the worsening of a health condition will be delayed; to inhibit the occurrence or recurrence of a health condition; to decrease the probability that a health condition will occur or reoccur; to delay the onset of a health condition; to increase the probability that the onset of a health condition will be delayed; to alleviate at least one symptom of a health condition; to increase the probability that at least one symptom of a health condition will be alleviated; to shorten the time over which at least one symptom of a health condition is alleviated; to increase the probability that the time necessary to alleviate at least one symptom of a health condition will be shortened; to decrease the severity of at least one symptom of a health condition; to increase the probability that the severity of at least one symptom of a health condition will be decreased; to shorten the time over which the severity of at least one symptom of a health condition is decreased; to increase the probability that the time necessary to decrease the severity of at least one symptom of a health condition will be shortened; to inhibit at least one symptom of a health condition from worsening; to increase the probability that at least one symptom of a health condition will not worsen; to delay the worsening of at least one symptom of a health condition; to increase the probability that the worsening of at least one symptom of a health condition will be delayed; to inhibit at least one symptom of a health condition from occurring or reoccurring; to decrease the probability that at least one symptom of a health condition will occur or reoccur; to delay the onset of at least one symptom of a health condition; and to increase the probability that the onset of at least one symptom of a health condition will be delayed.

In some embodiments, the health condition is epilepsy, anxiety, pain, or inflammation.

In some embodiments, the active ingredient is a cannabinoid.

In some embodiments, the active ingredient is a molecule selected from CBD, THC, A8-THC, CBG, CBDV, THCV, Δ8-THCV, CBGV, CBN, tetrahydrocannabiphorol, perrottetinene, nabilone, parahexyl, HUM-217, and HU-331; and the molecule has an acid dissociation constant in water for conversion of the molecule into the anion.

In some embodiments, the active ingredient is an anion; and a molecule selected from CBD, THC, Δ8-THC, CBG, CBDV, THCV, Δ8-THCV, CBGV, CBN, tetrahydrocannabiphorol, perrottetinene, nabilone, parahexyl, HUM-217, and HU-331 has an acid dissociation constant in water for conversion of the molecule into the anion.

In some embodiments, the molecule is CBD.

In some embodiments, the molecule is THC.

In some embodiments, the anion has the general structure I, II, or III; each skeletal atom is a carbon atom except that each asterisk (*) depicts an independent, optional substitution of a skeletal atom with either an oxygen atom, a sulfur atom, a sulfinyl, a sulfonyl, or a nitrogen atom; each cross (†) depicts an optional R group, which occurs for each odd-numbered R group that is bonded to a skeletal atom that is either a carbon atom or a nitrogen atom, which is omitted for each odd-numbered R group that is bonded to an oxygen atom, a sulfur atom, a sulfinyl, or a sulfonyl, which occurs for each even-numbered R group that is bonded to a skeletal atom that is a saturated carbon atom, and which is omitted for each even-numbered R group that is bonded to a skeletal atom that is an unsaturated carbon atom; exactly one R group is oxide, and this R group is selected such that the oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond; each dotted line depicts an optional double bond; an optional implicit hydrogen atom is bonded to each skeletal atom that is a carbon atom that is not bonded to an even-numbered R group; optional double bonds are selected and optional implicit hydrogen atoms are selected such that (i) the R group that is oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond, and (ii) no skeletal atom carries a full charge; and each R group is selected such that the anion comprises (i) at least 6 and no greater than 45 carbon atoms, (ii) at least 5 and no greater than 60 hydrogen atoms, (iii) at least 1 and no greater than 12 oxygen atoms, and (iv) no greater than 6 total combined sulfur, nitrogen, and halogen atoms.

Odd-numbered R groups comprise R1, R3, R5, R7, R9, R11, R21, R23, R25, R27, R29, R35, R37, and R39. Even-numbered R groups comprise R4, R8, R34, and R36.

The following exemplification sets forth specific embodiments that do not limit the preceding disclosure or any claim that matures from this patent document.

EXEMPLIFICATION

The activity of formulations set forth in this disclosure is assayed in Sabra mice. 300 milligrams of a formulation is combined with 15 milliliters of water and administered by oral gavage. Each formulation comprises a liquid phase that contains propylene glycol and a solid phase that contains xylitol. The liquid phase contains a cannabinoid selected from CBD, THC, Δ8-THC, CBG, CBDV, THCV, Δ8-THCV, CBGV, CBC, CBN, tetrahydrocannabiphorol, perrottetinene, nabilone, parahexyl, HUM-217, and HU-331, which is dissolved in the propylene glycol, and controls lack any cannabinoid.

Zymosan is injected into the left hind paws of each mouse to induce pain, inflammation, and tumor necrosis factor (“TNF”) signaling. Inflammatory paw swelling is measured with a caliper. Pain is measured with a Von Frey hair aesthesiometer. Plasma TNF is measured by HPLC. Formulations containing CBD, CBDV, HUM-217, and HU-331 each display robust reduction in pain, inflammation, and TNF signaling relative to controls. Formulations containing THC, Δ8-THC, CBG, THCV, Δ8-THCV, CBN, tetrahydrocannabiphorol, perrottetinene, nabilone, and parahexyl each display modest reduction in pain, inflammation, and TNF signaling relative to controls. The formulation containing CBC displays no detectable effect on pain, inflammation, and TNF signaling relative to controls. 

The invention claimed is:
 1. A composition, comprising a solid phase and a liquid phase, wherein the solid phase has a surface-area-to-volume ratio that is greater than 500 per meter; the solid phase consists of ingredients; the ingredients of the solid phase comprise carbohydrates; the carbohydrates comprise one or more of alginic acid, alginate, propylene glycol alginate, inulin, arabinogalactan, lignosulfonate, carrageenan, furcelleran, pullulan, glucomannan, gellan gum, gum arabic, gellan gum, gum ghatti, guar gum, gum karaya, tara gum, tragacanth, xanthan gum, carboxymethylcellulose, hydroxyethyl cellulose, ethylhydroxyethylcellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, modified starch, dextrin, polydextrose, pectin, beta-glucan, lactobionic acid, lactobionate, isomalt, erythritol, threitol, arabitol, xylitol, ribitol, mannitol, sorbitol, galactitol, fucitol, iditol, inositol, volemitol, sucrose, lactose, maltose, trehalose, maltitol, glucose, fructose, galactose, arabinose, ribose, xylose, allulose, sorbose, tagatose, fucose, mannose, and hydrogenated starch hydrolysate; at least 90 percent of the ingredients of the solid phase consist of the carbohydrates by mass; the composition comprises the liquid phase at a concentration of at least 0.5 percent and no greater than 15 percent by mass; the composition comprises the solid phase at a concentration of at least 85 percent and no greater than 99.5 percent by mass; the composition comprises at least 2 and no greater than 4 calories of food energy per gram of the composition; the liquid phase comprises a concentration of calories of food energy per gram of the liquid phase; the solid phase comprises a concentration of calories of food energy per gram of the solid phase that is less than the concentration of calories of food energy per gram of the liquid phase; the liquid phase consists of ingredients that comprise a solvent; each of the ingredients of the liquid phase has a concentration by mass in the liquid phase; the concentration by mass of the solvent in the liquid phase is greater than the concentration by mass of any of the other ingredients of the liquid phase; and the solvent is propane-1,2-diol.
 2. A container that contains at least 100 milligrams and no greater than 5 grams of a composition, wherein the composition comprises a solid phase and a liquid phase; the solid phase has a surface-area-to-volume ratio that is greater than 500 per meter; the solid phase consists of ingredients; the ingredients of the solid phase comprise carbohydrates; the carbohydrates comprise one or more sugar alcohols; at least 90 percent of the ingredients of the solid phase consist of the carbohydrates by mass; the composition comprises the liquid phase at a concentration of at least 0.5 percent and no greater than 15 percent by mass; the composition comprises the solid phase at a concentration of at least 85 percent and no greater than 99.5 percent by mass; the composition comprises at least 2 and no greater than 4 calories of food energy per gram of the composition; the liquid phase comprises a concentration of calories of food energy per gram of the liquid phase; the solid phase comprises a concentration of calories of food energy per gram of the solid phase that is less than the concentration of calories of food energy per gram of the liquid phase; the liquid phase consists of ingredients that comprise a solvent; each of the ingredients of the liquid phase has a concentration by mass in the liquid phase; the concentration by mass of the solvent in the liquid phase is greater than the concentration by mass of any of the other ingredients of the liquid phase; the solvent is propane-1,2-diol; the ingredients of the liquid phase comprise an active ingredient; the active ingredient is a solute that is dissolved in the solvent of the liquid phase; the active ingredient is dissolved in the solvent of the liquid phase at a concentration of at least 200 micromolar and no greater than 250 millimolar; the active ingredient has a solubility in water at 37 degrees Celsius; the active ingredient is dissolved in the solvent of the liquid phase at a concentration that is greater than the solubility of the active ingredient in water at 37 degrees Celsius; and the active ingredient has an octanol-water partition coefficient of at least
 10. 3. A method to prepare a beverage formulation, comprising providing a composition comprising an active ingredient; providing a beverage; and combining the composition with the beverage to disperse the active ingredient in the beverage and to prepare the beverage formulation, wherein the composition comprises a solid phase and a liquid phase; the solid phase has a surface-area-to-volume ratio that is greater than 500 per meter; the solid phase consists of ingredients; the ingredients of the solid phase comprise carbohydrates; at least 90 percent of the ingredients of the solid phase consist of the carbohydrates by mass; the composition comprises the liquid phase at a concentration of at least 0.5 percent and no greater than 15 percent by mass; the composition comprises the solid phase at a concentration of at least 85 percent and no greater than 99.5 percent by mass; the composition comprises at least 0.5 and no greater than 5 calories of food energy per gram of the composition; the liquid phase comprises a concentration of calories of food energy per gram of the liquid phase; the solid phase comprises a concentration of calories of food energy per gram of the solid phase that is less than the concentration of calories of food energy per gram of the liquid phase; the liquid phase consists of ingredients that comprise a solvent; each of the ingredients of the liquid phase has a concentration by mass in the liquid phase; the concentration by mass of the solvent in the liquid phase is greater than the concentration by mass of any of the other ingredients of the liquid phase; the solvent is propane-1,2-diol; the ingredients of the liquid phase comprise the active ingredient; the active ingredient is a solute that is dissolved in the solvent of the liquid phase; the active ingredient is dissolved in the solvent of the liquid phase at a concentration of at least 200 micromolar and no greater than 250 millimolar; the active ingredient has a solubility in water at 37 degrees Celsius; the active ingredient is dissolved in the solvent of the liquid phase at a concentration that is greater than the solubility of the active ingredient in water at 37 degrees Celsius; the active ingredient has an octanol-water partition coefficient of at least 10; and the beverage is a liquid that comprises water at a concentration of at least 50 molar.
 4. The method of claim 3, wherein the composition has a color; the beverage is colorless; and the beverage formulation has a color that is different from the color of the composition.
 5. The method of claim 3 or 4, wherein the ingredients of the liquid phase comprise a curcumin derivative selected from 5-hydroxy-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-2,4-diene-3-oxide; 5-hydroxy-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-2,5-diene-3-oxide; 5-hydroxy-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-3,5-diene-3-oxide; 5-oxo-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hept-2-ene-3-oxide; 5-oxo-1,7-bis(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hept-3-ene-3-oxide; 2-methoxy-4-[3-hydroxy-5-oxo-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3-dienyl]phenolate; 2-methoxy-4-[5-hydroxy-3-oxo-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,4-dienyl]phenolate; 2-methoxy-4-[5-hydroxy-3-oxo-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,5-dienyl]phenolate; 2-methoxy-4-[3,5-dioxo-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hept-1-en-1-yl]phenolate; 2-methoxy-4-[3,5-dihydroxy-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3,5-trienyl]phenolate; 5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3,5-triene-3-oxide; 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3,5-triene-5-oxide; 5-oxo-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,3-diene-3-oxide; 3-oxo-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,4-diene-5-oxide; 3-oxo-1-(4-hydroxy-3-methoxyphenyl)-7-(3-methoxy-4-oxocyclohexa-2,5-dienylidene)hepta-1,5-diene-5-oxide; 2-methoxy-4-[3-hydroxy-5-oxo-7-(4-hydroxy-3-methoxyphenyl)hepta-1,3,6-trienyl]phenolate; 2-methoxy-4-[5-hydroxy-3-oxo-7-(4-hydroxy-3-methoxyphenyl)hepta-1,4,6-trienyl]phenolate; and 2-methoxy-4-[3,5-dioxo-7-(4-hydroxy-3-methoxyphenyl)hepta-1,6-dienyl]phenolate.
 6. The method of any one of claims 3-5, comprising recording video or images of the composition both prior to and subsequent to combining the composition with the beverage.
 7. A method to market a composition, comprising disseminating over the internet the video or images recorded according to the method of claim
 6. 8. The method of any one of claims 3-7, wherein the ingredients of the liquid phase comprise one or both of 1-hydroxypropane-2-oxide and 2-hydroxypropane-1-oxide.
 9. The method of any one of claims 3-8, wherein the liquid phase comprises propane-1,2-diol and one or both of 1-hydroxypropane-2-oxide and 2-hydroxypropane-1-oxide at a molar ratio of at least 100:1 and no greater than 1,000,000:1 (propane-1,2-diol:1-hydroxypropane-2-oxide and 2-hydroxypropane-1-oxide).
 10. The method of any one of claims 3-9, comprising combining at least 100 milligrams and no greater than 5 grams of the composition with the beverage.
 11. The method of any one of claims 3-10, wherein the composition comprises at least 10 micrograms and no greater than 100 milligrams of the active ingredient.
 12. The method of any one of claims 3-11, comprising administering the beverage formulation to a human, wherein the human self-administers the beverage formulation by drinking it.
 13. The method of claim 12, wherein the human presents with a health condition, and the composition comprises an amount of the active ingredient that is effective to treat the health condition.
 14. The method of claim 13, wherein the health condition is epilepsy, anxiety, pain, or inflammation.
 15. The method of any one of claims 3-14, wherein the active ingredient is a cannabinoid.
 16. The method of any one of claims 3-15, wherein the active ingredient is a molecule selected from CBD, THC, Δ8-THC, CBG, CBDV, THCV, Δ8-THCV, CBGV, CBN, tetrahydrocannabiphorol, perrottetinene, nabilone, parahexyl, HUM-217, and HU-331; and the molecule has an acid dissociation constant in water for conversion of the molecule into the anion.
 17. The method of any one of claims 3-15, wherein the active ingredient is an anion; and a molecule selected from CBD, THC, Δ8-THC, CBG, CBDV, THCV, Δ8-THCV, CBGV, CBN, tetrahydrocannabiphorol, perrottetinene, nabilone, parahexyl, HUM-217, and HU-331 has an acid dissociation constant in water for conversion of the molecule into the anion.
 18. The method of claim 16 or 17, wherein the molecule is CBD.
 19. The method of claim 16 or 17, wherein the molecule is THC.
 20. The method of any one of claims 16-19, wherein the anion has the general structure I, II, or III

each skeletal atom is a carbon atom except that each asterisk (*) depicts an independent, optional substitution of a skeletal atom with either an oxygen atom, a sulfur atom, a sulfinyl, a sulfonyl, or a nitrogen atom; each cross (†) depicts an optional R group, which occurs for each odd-numbered R group that is bonded to a skeletal atom that is either a carbon atom or a nitrogen atom, which is omitted for each odd-numbered R group that is bonded to an oxygen atom, a sulfur atom, a sulfinyl, or a sulfonyl, which occurs for each even-numbered R group that is bonded to a skeletal atom that is a saturated carbon atom, and which is omitted for each even-numbered R group that is bonded to a skeletal atom that is an unsaturated carbon atom; exactly one R group is oxide, and this R group is selected such that the oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond; each dotted line depicts an optional double bond; an optional implicit hydrogen atom is bonded to each skeletal atom that is a carbon atom that is not bonded to an even-numbered R group; optional double bonds are selected and optional implicit hydrogen atoms are selected such that (i) the R group that is oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond, and (ii) no skeletal atom carries a full charge; and each R group is selected such that the anion comprises (i) at least 6 and no greater than 45 carbon atoms, (ii) at least 5 and no greater than 60 hydrogen atoms, (iii) at least 1 and no greater than 12 oxygen atoms, and (iv) no greater than 6 total combined sulfur, nitrogen, and halogen atoms.
 21. The method of claim 20, wherein each R group that occurs, other than the R group that is oxide, is independently selected from H; a halogen; hydroxy; amino; oxo; formyl; isocyano; carbamoyl; nitro; a substituted or unsubstituted C3-C10 cycloalkyl, aryl, arylalkyl, arylcarbonyl, arylcarbonyloxy, arylcarbonylamino, aryloxycarbonyl, arylcarbamoyl, arylalkylcarbonyl, arylalkylcarbonyloxy, arylalkylcarbonylamino, arylalkyloxycarbonyl, or arylalkylcarbamoyl; and a substituted orunsubstituted, straight-or-branched C1-C12 alkyl, alkylidene, alkyloxy, alkylsulfanyl, alkylamino, alkylcarbonyl, alkylcarbonyloxy, alkylcarbonylsulfanyl, alkylcarbonylamino, alkyloxycarbonyl, alkylsulfanylcarbonyl, or alkylcarbamoyl, wherein substituted refers to at least one of, in any order and without limitation, (i) the substitution of two hydrogen atoms with a double bond, (ii) the substitution of a double bond with two hydrogen atoms, (iii) the substitution of a hydrogen atom with a halogen; hydroxy; amino; formyl; isocyano; carbamoyl; nitro; a substituted or unsubstituted C3-C10 cycloalkyl, aryl, arylalkyl, arylcarbonyl, arylcarbonyloxy, arylcarbonylamino, aryloxycarbonyl, arylcarbamoyl, arylalkylcarbonyl, arylalkylcarbonyloxy, arylalkylcarbonylamino, arylalkyloxycarbonyl, or arylalkylcarbamoyl; or a substituted or unsubstituted, straight-or-branched C1-C12 alkyl, alkylidene, alkyloxy, alkylsulfanyl, alkylamino, alkylcarbonyl, alkylcarbonyloxy, alkylcarbonylsulfanyl, alkylcarbonylamino, alkyloxycarbonyl, alkylsulfanylcarbonyl, or alkylcarbamoyl, (iv) the substitution of two hydrogen atoms with methylene, epoxy, or a substituted or unsubstituted, straight-or-branched C1-C12 alkyl such that the substitution of the two hydrogen atoms forms a cycle that consists of 3 to 14 atoms, (v) the substitution of two hydrogen atoms with either oxo or a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene, and (vi) the substitution of a methylene bridge (—CH₂—) with an oxygen atom, a sulfur atom, sulfinyl, sulfonyl, a protonated nitrogen atom, or a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino, except that two R groups may be optionally co-selected from methylene, epoxy, or a substituted or unsubstituted, straight-or-branched C1-C12 alkyl such that the two R groups form cycle that consists of 3 to 14 atoms.
 22. The method of claim 20 or 21, wherein each skeletal atom is a carbon atom except that one or two asterisks (*) depict an independent, optional substitution of a skeletal atom with either an oxygen atom; each R group that occurs, other than the R group that is oxide, is independently selected from H; a halogen; hydroxy; oxo; formyl; a substituted or unsubstituted C3-C10 cycloalkyl, aryl, or arylalkyl; and a substituted or unsubstituted, straight-or-branched C1-C12 alkyl, alkyloxy, alkylcarbonyl, alkyloxycarbonyl, or alkylcarbonyloxy, wherein substituted is limited to (i) the substitution of two hydrogen atoms with a double bond, oxo, methylidene, methylene, epoxy, or methylenedioxy (ii) the substitution of a double bond with two hydrogen atoms, (iii) the substitution of a hydrogen atom with a halogen; hydroxy; or a substituted or unsubstituted methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octanyl, nonanyl, decanyl, undecanyl, dodecanyl, cyclohexyl, phenyl, benzyl, 4H-chromen-2-yl, or 4H-chromen-3-yl, and (vi) the substitution of a methylene bridge with an oxygen atom, except that two R groups may be co-selected from methylene, epoxy, and methylenedioxy.
 23. The method of any one of claims 20-22, wherein each R group that occurs, other than the R group that is oxide, is independently selected from H; methyl; ethyl; propyl; butyl; pentyl; hexyl; heptyl; ethenyl; ethynyl; prop-1-enyl; propen-2-yl; prenyl; geranyl; a halogen; hydroxy; methoxy; ethoxy; 2-propoxy; oxo; formyl; acetyl; propionyl; 2-oxo-propyl; butyryl; 3-oxo-butyl; phenyl; benzyl; phenylcarbonyl; 2-phenylethyl; 2-phenylethenyl; 3-phenylprop-2-enonyl; and a methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, acetyl, propionyl, 2-oxo-propyl, butyryl, 3-oxo-butyl, phenyl, benzyl, phenylcarbonyl, 2-phenylethyl, 2-phenylethenyl, or 3-phenylprop-2-enonyl that is substituted with 1, 2, or 3 groups selected from methyl, ethyl, propyl, a halogen, hydroxy, methoxy, ethoxy, and 2-propoxy.
 24. The method of any one of claims 16-23, wherein the anion has the general structure I

each skeletal atom is a carbon atom; exactly one R group is oxide, and this R group is selected such that the oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond; each dotted line depicts an optional double bond; optional double bonds are selected such that (i) the R group that is oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond, and (ii) no skeletal atom carries a full charge; and each R group is selected such that the anion comprises (i) at least 6 and no greater than 45 carbon atoms, (ii) at least 5 and no greater than 60 hydrogen atoms, (iii) at least 1 and no greater than 12 oxygen atoms, and (iv) no greater than 6 total combined sulfur, nitrogen, and halogen atoms
 25. The method of any one of claims 16-23, wherein the anion has the general structure II

each skeletal atom is a carbon atom; exactly one R group is oxide, and this R group is selected such that the oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond; each dotted line depicts an optional double bond; optional double bonds are selected such that (i) the R group that is oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond, and (ii) no skeletal atom carries a full charge; and each R group is selected such that the anion comprises (i) at least 6 and no greater than 45 carbon atoms, (ii) at least 5 and no greater than 60 hydrogen atoms, (iii) at least 1 and no greater than 12 oxygen atoms, and (iv) no greater than 6 total combined sulfur, nitrogen, and halogen atoms
 26. The method of claim 25, wherein the dotted lines labeled with B1, B3, B5, B7, B9, and B11 depict single bonds.
 27. The method of claim 25, wherein the dotted line labeled with B1 depicts a double bond; and the dotted lines labeled with B3, B5, B7, B9, and B11 depict single bonds.
 28. The method of claim 25, wherein the dotted line labeled with B3 depicts a double bond; and the dotted lines labeled with B1, B5, B7, B9, and B11 depict single bonds.
 29. The method of claim 25, wherein the dotted line labeled with B5 depicts a double bond; and the dotted lines labeled with B1, B3, B7, B9, and B11 depict single bonds.
 30. The method of claim 25, wherein the dotted line labeled with B7 depicts a double bond; and the dotted lines labeled with B1, B3, B5, B9, and B11 depict single bonds.
 31. The method of claim 25, wherein the dotted line labeled with B9 depicts a double bond; and the dotted lines labeled with B1, B3, B5, B7, and B11 depict single bonds.
 32. The method of claim 25, wherein the dotted line labeled with B11 depicts a double bond; and the dotted lines labeled with B1, B3, B5, B7, and B9 depict single bonds.
 33. The method of any one of claims 25-32, wherein the dotted line labeled with AA depicts a single bond.
 34. The method of any one of claims 25-33, wherein R21 is H.
 35. The method of any one of claims 25-33, wherein R21 is a halogen.
 36. The method of any one of claims 25-33, wherein R21 is hydroxy.
 37. The method of any one of claims 25-33, wherein R21 is amino.
 38. The method of any one of claims 25-33, wherein R21 is oxo.
 39. The method of any one of claims 25-33, wherein R21 is formyl.
 40. The method of any one of claims 25-33, wherein R21 is isocyano.
 41. The method of any one of claims 25-33, wherein R21 is carbamoyl.
 42. The method of any one of claims 25-33, wherein R21 is nitro.
 43. The method of any one of claims 25-33, wherein R21 is ethenyl.
 44. The method of any one of claims 25-33, wherein R21 is ethynyl.
 45. The method of any one of claims 25-33, wherein R21 is prop-1-enyl.
 46. The method of any one of claims 25-33, wherein R21 is propen-2-yl.
 47. The method of any one of claims 25-33, wherein R21 is prenyl.
 48. The method of any one of claims 25-33, wherein R21 is geranyl.
 49. The method of any one of claims 25-33, wherein R21 is methoxy.
 50. The method of any one of claims 25-33, wherein R21 is ethoxy.
 51. The method of any one of claims 25-33, wherein R21 is 2-propoxy.
 52. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted methyl.
 53. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted ethyl.
 54. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted propyl.
 55. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted butyl.
 56. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted pentyl.
 57. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted hexyl.
 58. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted heptyl.
 59. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted acetyl.
 60. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted propionyl.
 61. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted 2-oxo-propyl.
 62. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted butyryl.
 63. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted 3-oxo-butyl.
 64. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted phenyl.
 65. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted benzyl.
 66. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted phenylcarbonyl.
 67. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted 2-phenylethyl.
 68. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted 2-phenylethenyl.
 69. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 70. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 cycloalkyl.
 71. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 aryl.
 72. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylalkyl.
 73. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 74. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 75. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 76. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 77. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 78. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 79. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 80. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 81. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 82. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 83. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 84. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 85. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 86. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 87. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 88. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 89. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 90. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 91. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 92. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 93. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 94. The method of any one of claims 25-33, wherein R21 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 95. The method of any one of claims 25-94, wherein R29 is H.
 96. The method of any one of claims 25-94, wherein R29 is a halogen.
 97. The method of any one of claims 24-96, wherein the dotted lines labeled with A1, A5, and A9 depict double bonds; and the dotted lines labeled with A3, A7, and A11 depict single bonds.
 98. The method of any one of claims 24-96, wherein the dotted lines labeled with A3, A7, and A11 depict double bonds; and the dotted lines labeled with A1, A5, and A9 depict single bonds.
 99. The method of any one of claims 24-96, wherein the dotted lines labeled with A3 and A11 depict double bonds; and the dotted lines labeled with A1, A5, A7, and A9 depict single bonds.
 100. The method of claim 99, wherein R7 is oxo and R9 is oxo.
 101. The method of any one of claims 24-96, wherein the dotted lines labeled with A5 and A11 depict double bonds; and the dotted lines labeled with A1, A3, A7, and A9 depict single bonds.
 102. The method of claim 101, wherein R3 is oxo and R9 is oxo.
 103. The method of any one of claims 24-102, wherein R1 is oxide.
 104. The method of any one of claims 16-23, wherein the anion has the general structure III

each skeletal atom is a carbon atom except that each asterisk (*) depicts an independent, optional substitution of a skeletal atom with an oxygen atom; each cross (†) depicts an optional R group, which occurs for each odd-numbered R group that is bonded to a skeletal atom that is a carbon atom, which is omitted for each odd-numbered R group that is bonded to an oxygen atom, which occurs for each even-numbered R group that is bonded to a skeletal atom that is a saturated carbon atom, and which is omitted for each even-numbered R group that is bonded to a skeletal atom that is an unsaturated carbon atom; exactly one R group is oxide, and this R group is selected such that the oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond; each dotted line depicts an optional double bond; an optional implicit hydrogen atom is bonded to each skeletal atom that is a carbon atom that is not bonded to an even-numbered R group; optional double bonds are selected and optional implicit hydrogen atoms are selected such that (i) the R group that is oxide is covalently bound to a carbon atom of an aromatic ring or an otherwise unsaturated carbon atom by a single bond, and (ii) no skeletal atom carries a full charge; and each R group is selected such that the anion comprises (i) at least 6 and no greater than 45 carbon atoms, (ii) at least 5 and no greater than 60 hydrogen atoms, (iii) at least 1 and no greater than 12 oxygen atoms, and (iv) no greater than 6 total combined sulfur, nitrogen, and halogen atoms
 105. The method of claim 104, wherein exactly one skeletal atom that is marked with an asterisk (*) is substituted with oxygen.
 106. The method of claim 104 or 105, wherein exactly one skeletal atom that is marked with an asterisk (*) is substituted with oxygen, and the exactly one skeletal atom that is marked with an asterisk (*) and substituted with oxygen is the skeletal atom that participates in both the bond depicted by the dotted line labeled with A1 and the bond depicted by the dotted lines labeled with A11.
 107. The method of any one of claims 104-106, wherein R1 is omitted.
 108. The method of any one of claims 104-107, wherein the dotted line labeled with A5 depicts a double bond; and the dotted lines labeled with C1, C3, C5, C7, and C9 depict single bonds.
 109. The method of any one of claims 104-107, wherein the dotted line labeled with C1 depicts a double bond; and the dotted lines labeled with A5, C3, C5, C7, and C9 depict single bonds.
 110. The method of any one of claims 104-107, wherein the dotted line labeled with C3 depicts a double bond; and the dotted lines labeled with A5, C1, C5, C7, and C9 depict single bonds.
 111. The method of any one of claims 104-107, wherein the dotted line labeled with C5 depicts a double bond; and the dotted lines labeled with A5, C1, C3, C7, and C9 depict single bonds.
 112. The method of any one of claims 104-107, wherein the dotted line labeled with C7 depicts a double bond; and the dotted lines labeled with A5, C1, C3, C5, and C9 depict single bonds.
 113. The method of any one of claims 104-107, wherein the dotted line labeled with C9 depicts a double bond; and the dotted lines labeled with A5, C1, C3, C5, and C7 depict single bonds.
 114. The method of any one of claims 104-107, wherein the dotted lines labeled with A5, C3, and C7 depict double bonds; and the dotted lines labeled with C1, C5, and C9 depict single bonds.
 115. The method of any one of claims 104-107, wherein the dotted lines labeled with A5, C1, C3, C5, C7, and C9 depict single bonds.
 116. The method of any one of claims 104-115, wherein the dotted lines labeled with A9, B1, and B5 depict double bonds, and the dotted lines labeled with B3, B7, and B11 depict single bonds.
 117. The method of any one of claims 104-115, wherein the dotted lines labeled with B3, B7, and B11 depict double bonds, and the dotted lines labeled with A9, B1, and B5 depict single bonds.
 118. The method of any one of claims 104-117, wherein the dotted lines labeled with A1, A3, A7, and A11 depict single bonds.
 119. The method of any one of claims 104-118, wherein R21 is oxide.
 120. The method of any one of claims 104-119, wherein R4 is H.
 121. The method of any one of claims 104-119, wherein R4 is a halogen.
 122. The method of any one of claims 104-119, wherein R4 is hydroxy.
 123. The method of any one of claims 104-119, wherein R4 is formyl.
 124. The method of any one of claims 104-119, wherein R4 is isocyano.
 125. The method of any one of claims 104-119, wherein R4 is carbamoyl.
 126. The method of any one of claims 104-119, wherein R4 is nitro.
 127. The method of any one of claims 104-119, wherein R4 is ethenyl.
 128. The method of any one of claims 104-119, wherein R4 is ethynyl.
 129. The method of any one of claims 104-119, wherein R4 is prop-1-enyl.
 130. The method of any one of claims 104-119, wherein R4 is propen-2-yl.
 131. The method of any one of claims 104-119, wherein R4 is prenyl.
 132. The method of any one of claims 104-119, wherein R4 is geranyl.
 133. The method of any one of claims 104-119, wherein R4 is methoxy.
 134. The method of any one of claims 104-119, wherein R4 is ethoxy.
 135. The method of any one of claims 104-119, wherein R4 is 2-propoxy.
 136. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted methyl.
 137. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted ethyl.
 138. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted propyl.
 139. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted butyl.
 140. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted pentyl.
 141. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted hexyl.
 142. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted heptyl.
 143. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted acetyl.
 144. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted propionyl.
 145. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted 2-oxo-propyl.
 146. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted butyryl.
 147. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted 3-oxo-butyl.
 148. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted phenyl.
 149. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted benzyl.
 150. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted phenylcarbonyl.
 151. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted 2-phenylethyl.
 152. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted 2-phenylethenyl.
 153. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 154. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 cycloalkyl.
 155. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 aryl.
 156. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylalkyl.
 157. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 158. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 159. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 160. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 161. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 162. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 163. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 164. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 165. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 166. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 167. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 168. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 169. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 170. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 171. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 172. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 173. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 174. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 175. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 176. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 177. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 178. The method of any one of claims 104-119, wherein R4 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 179. The method of any one of claims 104-119, wherein R4 is omitted.
 180. The method of any one of claims 104-179, wherein R8 is H.
 181. The method of any one of claims 104-179, wherein R8 is omitted.
 182. The method of any one of claims 104-181, wherein R33 is H.
 183. The method of any one of claims 104-181, wherein R33 is a halogen.
 184. The method of any one of claims 104-181, wherein R33 is hydroxy.
 185. The method of any one of claims 104-181, wherein R33 is amino.
 186. The method of any one of claims 104-181, wherein R33 is oxo.
 187. The method of any one of claims 104-181, wherein R33 is formyl.
 188. The method of any one of claims 104-181, wherein R33 is isocyano.
 189. The method of any one of claims 104-181, wherein R33 is carbamoyl.
 190. The method of any one of claims 104-181, wherein R33 is nitro.
 191. The method of any one of claims 104-181, wherein R33 is ethenyl.
 192. The method of any one of claims 104-181, wherein R33 is ethynyl.
 193. The method of any one of claims 104-181, wherein R33 is prop-1-enyl.
 194. The method of any one of claims 104-181, wherein R33 is propen-2-yl.
 195. The method of any one of claims 104-181, wherein R33 is prenyl.
 196. The method of any one of claims 104-181, wherein R33 is geranyl.
 197. The method of any one of claims 104-181, wherein R33 is methoxy.
 198. The method of any one of claims 104-181, wherein R33 is ethoxy.
 199. The method of any one of claims 104-181, wherein R33 is 2-propoxy.
 200. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted methyl.
 201. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted ethyl.
 202. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted propyl.
 203. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted butyl.
 204. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted pentyl.
 205. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted hexyl.
 206. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted heptyl.
 207. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted acetyl.
 208. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted propionyl.
 209. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted 2-oxo-propyl.
 210. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted butyryl.
 211. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted 3-oxo-butyl.
 212. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted phenyl.
 213. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted benzyl.
 214. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted phenylcarbonyl.
 215. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted 2-phenylethyl.
 216. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted 2-phenylethenyl.
 217. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 218. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 cycloalkyl.
 219. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 aryl.
 220. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylalkyl.
 221. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 222. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 223. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 224. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 225. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 226. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 227. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 228. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 229. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 230. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 231. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 232. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 233. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 234. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 235. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 236. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 237. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 238. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 239. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 240. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 241. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 242. The method of any one of claims 104-181, wherein R33 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 243. The method of any one of claims 104-242, wherein R34 is H.
 244. The method of any one of claims 104-242, wherein R34 is a halogen.
 245. The method of any one of claims 104-242, wherein R34 is hydroxy.
 246. The method of any one of claims 104-242, wherein R34 is amino.
 247. The method of any one of claims 104-242, wherein R34 is formyl.
 248. The method of any one of claims 104-242, wherein R34 is isocyano.
 249. The method of any one of claims 104-242, wherein R34 is carbamoyl.
 250. The method of any one of claims 104-242, wherein R34 is nitro.
 251. The method of any one of claims 104-242, wherein R34 is ethenyl.
 252. The method of any one of claims 104-242, wherein R34 is ethynyl.
 253. The method of any one of claims 104-242, wherein R34 is prop-1-enyl.
 254. The method of any one of claims 104-242, wherein R34 is propen-2-yl.
 255. The method of any one of claims 104-242, wherein R34 is prenyl.
 256. The method of any one of claims 104-242, wherein R34 is geranyl.
 257. The method of any one of claims 104-242, wherein R34 is methoxy.
 258. The method of any one of claims 104-242, wherein R34 is ethoxy.
 259. The method of any one of claims 104-242, wherein R34 is 2-propoxy.
 260. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted methyl.
 261. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted ethyl.
 262. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted propyl.
 263. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted butyl.
 264. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted pentyl.
 265. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted hexyl.
 266. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted heptyl.
 267. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted acetyl.
 268. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted propionyl.
 269. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted 2-oxo-propyl.
 270. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted butyryl.
 271. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted 3-oxo-butyl.
 272. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted phenyl.
 273. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted benzyl.
 274. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted phenylcarbonyl.
 275. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted 2-phenylethyl.
 276. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted 2-phenylethenyl.
 277. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 278. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 cycloalkyl.
 279. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 aryl.
 280. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylalkyl.
 281. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 282. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 283. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 284. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 285. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 286. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 287. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 288. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 289. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 290. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 291. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 292. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 293. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 294. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 295. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 296. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 297. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 298. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 299. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 300. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 301. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 302. The method of any one of claims 104-242, wherein R34 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 303. The method of any one of claims 104-242, wherein R34 is omitted.
 304. The method of any one of claims 104-303, wherein R35 is H.
 305. The method of any one of claims 104-303, wherein R35 is a halogen.
 306. The method of any one of claims 104-303, wherein R35 is hydroxy.
 307. The method of any one of claims 104-303, wherein R35 is amino.
 308. The method of any one of claims 104-303, wherein R35 is oxo.
 309. The method of any one of claims 104-303, wherein R35 is formyl.
 310. The method of any one of claims 104-303, wherein R35 is isocyano.
 311. The method of any one of claims 104-303, wherein R35 is carbamoyl.
 312. The method of any one of claims 104-303, wherein R35 is nitro.
 313. The method of any one of claims 104-303, wherein R35 is ethenyl.
 314. The method of any one of claims 104-303, wherein R35 is ethynyl.
 315. The method of any one of claims 104-303, wherein R35 is prop-1-enyl.
 316. The method of any one of claims 104-303, wherein R35 is propen-2-yl.
 317. The method of any one of claims 104-303, wherein R35 is prenyl.
 318. The method of any one of claims 104-303, wherein R35 is geranyl.
 319. The method of any one of claims 104-303, wherein R35 is methoxy.
 320. The method of any one of claims 104-303, wherein R35 is ethoxy.
 321. The method of any one of claims 104-303, wherein R35 is 2-propoxy.
 322. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted methyl.
 323. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted ethyl.
 324. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted propyl.
 325. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted butyl.
 326. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted pentyl.
 327. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted hexyl.
 328. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted heptyl.
 329. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted acetyl.
 330. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted propionyl.
 331. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted 2-oxo-propyl.
 332. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted butyryl.
 333. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted 3-oxo-butyl.
 334. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted phenyl.
 335. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted benzyl.
 336. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted phenylcarbonyl.
 337. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted 2-phenylethyl.
 338. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted 2-phenylethenyl.
 339. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 340. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 cycloalkyl.
 341. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 aryl.
 342. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylalkyl.
 343. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 344. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 345. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 346. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 347. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 348. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 349. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 350. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 351. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 352. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 353. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 354. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 355. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 356. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 357. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 358. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 359. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 360. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 361. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 362. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 363. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 364. The method of any one of claims 104-303, wherein R35 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 365. The method of any one of claims 104-364, wherein R36 is H.
 366. The method of any one of claims 104-364, wherein R36 is a halogen.
 367. The method of any one of claims 104-364, wherein R36 is hydroxy.
 368. The method of any one of claims 104-364, wherein R36 is amino.
 369. The method of any one of claims 104-364, wherein R36 is formyl.
 370. The method of any one of claims 104-364, wherein R36 is isocyano.
 371. The method of any one of claims 104-364, wherein R36 is carbamoyl.
 372. The method of any one of claims 104-364, wherein R36 is nitro.
 373. The method of any one of claims 104-364, wherein R36 is ethenyl.
 374. The method of any one of claims 104-364, wherein R36 is ethynyl.
 375. The method of any one of claims 104-364, wherein R36 is prop-1-enyl.
 376. The method of any one of claims 104-364, wherein R36 is propen-2-yl.
 377. The method of any one of claims 104-364, wherein R36 is prenyl.
 378. The method of any one of claims 104-364, wherein R36 is geranyl.
 379. The method of any one of claims 104-364, wherein R36 is methoxy.
 380. The method of any one of claims 104-364, wherein R36 is ethoxy.
 381. The method of any one of claims 104-364, wherein R36 is 2-propoxy.
 382. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted methyl.
 383. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted ethyl.
 384. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted propyl.
 385. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted butyl.
 386. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted pentyl.
 387. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted hexyl.
 388. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted heptyl.
 389. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted acetyl.
 390. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted propionyl.
 391. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted 2-oxo-propyl.
 392. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted butyryl.
 393. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted 3-oxo-butyl.
 394. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted phenyl.
 395. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted benzyl.
 396. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted phenylcarbonyl.
 397. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted 2-phenylethyl.
 398. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted 2-phenylethenyl.
 399. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 400. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 cycloalkyl.
 401. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 aryl.
 402. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylalkyl.
 403. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 404. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 405. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 406. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 407. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 408. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 409. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 410. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 411. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 412. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 413. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 414. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 415. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 416. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 417. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 418. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 419. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 420. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 421. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 422. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 423. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 424. The method of any one of claims 104-364, wherein R36 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 425. The method of any one of claims 104-364, wherein R36 is omitted.
 426. The method of any one of claims 104-425, wherein R37 is H.
 427. The method of any one of claims 104-425, wherein R37 is a halogen.
 428. The method of any one of claims 104-425, wherein R37 is hydroxy.
 429. The method of any one of claims 104-425, wherein R37 is amino.
 430. The method of any one of claims 104-425, wherein R37 is oxo.
 431. The method of any one of claims 104-425, wherein R37 is formyl.
 432. The method of any one of claims 104-425, wherein R37 is isocyano.
 433. The method of any one of claims 104-425, wherein R37 is carbamoyl.
 434. The method of any one of claims 104-425, wherein R37 is nitro.
 435. The method of any one of claims 104-425, wherein R37 is ethenyl.
 436. The method of any one of claims 104-425, wherein R37 is ethynyl.
 437. The method of any one of claims 104-425, wherein R37 is prop-1-enyl.
 438. The method of any one of claims 104-425, wherein R37 is propen-2-yl.
 439. The method of any one of claims 104-425, wherein R37 is prenyl.
 440. The method of any one of claims 104-425, wherein R37 is geranyl.
 441. The method of any one of claims 104-425, wherein R37 is methoxy.
 442. The method of any one of claims 104-425, wherein R37 is ethoxy.
 443. The method of any one of claims 104-425, wherein R37 is 2-propoxy.
 444. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted methyl.
 445. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted ethyl.
 446. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted propyl.
 447. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted butyl.
 448. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted pentyl.
 449. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted hexyl.
 450. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted heptyl.
 451. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted acetyl.
 452. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted propionyl.
 453. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted 2-oxo-propyl.
 454. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted butyryl.
 455. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted 3-oxo-butyl.
 456. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted phenyl.
 457. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted benzyl.
 458. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted phenylcarbonyl.
 459. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted 2-phenylethyl.
 460. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted 2-phenylethenyl.
 461. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 462. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 cycloalkyl.
 463. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 aryl.
 464. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylalkyl.
 465. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 466. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 467. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 468. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 469. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 470. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 471. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 472. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 473. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 474. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 475. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 476. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 477. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 478. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 479. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 480. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 481. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 482. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 483. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 484. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 485. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 486. The method of any one of claims 104-425, wherein R37 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 487. The method of any one of claims 104-486, wherein R39 is H.
 488. The method of any one of claims 104-486, wherein R39 is a halogen.
 489. The method of any one of claims 104-486, wherein R39 is hydroxy.
 490. The method of any one of claims 104-486, wherein R39 is amino.
 491. The method of any one of claims 104-486, wherein R39 is oxo.
 492. The method of any one of claims 104-486, wherein R39 is formyl.
 493. The method of any one of claims 104-486, wherein R39 is isocyano.
 494. The method of any one of claims 104-486, wherein R39 is carbamoyl.
 495. The method of any one of claims 104-486, wherein R39 is nitro.
 496. The method of any one of claims 104-486, wherein R39 is ethenyl.
 497. The method of any one of claims 104-486, wherein R39 is ethynyl.
 498. The method of any one of claims 104-486, wherein R39 is prop-1-enyl.
 499. The method of any one of claims 104-486, wherein R39 is propen-2-yl.
 500. The method of any one of claims 104-486, wherein R39 is prenyl.
 501. The method of any one of claims 104-486, wherein R39 is geranyl.
 502. The method of any one of claims 104-486, wherein R39 is methoxy.
 503. The method of any one of claims 104-486, wherein R39 is ethoxy.
 504. The method of any one of claims 104-486, wherein R39 is 2-propoxy.
 505. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted methyl.
 506. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted ethyl.
 507. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted propyl.
 508. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted butyl.
 509. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted pentyl.
 510. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted hexyl.
 511. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted heptyl.
 512. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted acetyl.
 513. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted propionyl.
 514. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted 2-oxo-propyl.
 515. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted butyryl.
 516. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted 3-oxo-butyl.
 517. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted phenyl.
 518. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted benzyl.
 519. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted phenylcarbonyl.
 520. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted 2-phenylethyl.
 521. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted 2-phenylethenyl.
 522. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 523. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 cycloalkyl.
 524. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 aryl.
 525. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylalkyl.
 526. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 527. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 528. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 529. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 530. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 531. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 532. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 533. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 534. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 535. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 536. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 537. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 538. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 539. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 540. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 541. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 542. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 543. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 544. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 545. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 546. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 547. The method of any one of claims 104-486, wherein R39 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 548. The method of any one of claims 25-547, wherein R23 is H.
 549. The method of any one of claims 25-547, wherein R23 is a halogen.
 550. The method of any one of claims 25-547, wherein R23 is hydroxy.
 551. The method of any one of claims 25-547, wherein R23 is amino.
 552. The method of any one of claims 25-547, wherein R23 is oxo.
 553. The method of any one of claims 25-547, wherein R23 is formyl.
 554. The method of any one of claims 25-547, wherein R23 is isocyano.
 555. The method of any one of claims 25-547, wherein R23 is carbamoyl.
 556. The method of any one of claims 25-547, wherein R23 is nitro.
 557. The method of any one of claims 25-547, wherein R23 is ethenyl.
 558. The method of any one of claims 25-547, wherein R23 is ethynyl.
 559. The method of any one of claims 25-547, wherein R23 is prop-1-enyl.
 560. The method of any one of claims 25-547, wherein R23 is propen-2-yl.
 561. The method of any one of claims 25-547, wherein R23 is prenyl.
 562. The method of any one of claims 25-547, wherein R23 is geranyl.
 563. The method of any one of claims 25-547, wherein R23 is methoxy.
 564. The method of any one of claims 25-547, wherein R23 is ethoxy.
 565. The method of any one of claims 25-547, wherein R23 is 2-propoxy.
 566. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted methyl.
 567. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted ethyl.
 568. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted propyl.
 569. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted butyl.
 570. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted pentyl.
 571. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted hexyl.
 572. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted heptyl.
 573. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted acetyl.
 574. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted propionyl.
 575. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted 2-oxo-propyl.
 576. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted butyryl.
 577. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted 3-oxo-butyl.
 578. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted phenyl.
 579. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted benzyl.
 580. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted phenylcarbonyl.
 581. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted 2-phenylethyl.
 582. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted 2-phenylethenyl.
 583. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 584. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 cycloalkyl.
 585. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 aryl.
 586. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylalkyl.
 587. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 588. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 589. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 590. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 591. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 592. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 593. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 594. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 595. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 596. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 597. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 598. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 599. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 600. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 601. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 602. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 603. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 604. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 605. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 606. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 607. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 608. The method of any one of claims 25-547, wherein R23 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 609. The method of any one of claims 25-608, wherein R25 is H.
 610. The method of any one of claims 25-608, wherein R25 is a halogen.
 611. The method of any one of claims 25-608, wherein R25 is hydroxy.
 612. The method of any one of claims 25-608, wherein R25 is amino.
 613. The method of any one of claims 25-608, wherein R25 is oxo.
 614. The method of any one of claims 25-608, wherein R25 is formyl.
 615. The method of any one of claims 25-608, wherein R25 is isocyano.
 616. The method of any one of claims 25-608, wherein R25 is carbamoyl.
 617. The method of any one of claims 25-608, wherein R25 is nitro.
 618. The method of any one of claims 25-608, wherein R25 is ethenyl.
 619. The method of any one of claims 25-608, wherein R25 is ethynyl.
 620. The method of any one of claims 25-608, wherein R25 is prop-1-enyl.
 621. The method of any one of claims 25-608, wherein R25 is propen-2-yl.
 622. The method of any one of claims 25-608, wherein R25 is prenyl.
 623. The method of any one of claims 25-608, wherein R25 is geranyl.
 624. The method of any one of claims 25-608, wherein R25 is hydroxy.
 625. The method of any one of claims 25-608, wherein R25 is methoxy.
 626. The method of any one of claims 25-608, wherein R25 is ethoxy.
 627. The method of any one of claims 25-608, wherein R25 is 2-propoxy.
 628. The method of any one of claims 25-608, wherein R25 is formyl.
 629. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted methyl.
 630. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted ethyl.
 631. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted propyl.
 632. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted butyl.
 633. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted pentyl.
 634. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted hexyl.
 635. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted heptyl.
 636. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted acetyl.
 637. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted propionyl.
 638. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted 2-oxo-propyl.
 639. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted butyryl.
 640. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted 3-oxo-butyl.
 641. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted phenyl.
 642. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted benzyl.
 643. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted phenylcarbonyl.
 644. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted 2-phenylethyl.
 645. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted 2-phenylethenyl.
 646. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 647. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 cycloalkyl.
 648. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 aryl.
 649. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylalkyl.
 650. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 651. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 652. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 653. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 654. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 655. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 656. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 657. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 658. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 659. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 660. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 661. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 662. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 663. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 664. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 665. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 666. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 667. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 668. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 669. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 670. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 671. The method of any one of claims 25-608, wherein R25 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 672. The method of any one of claims 25-671, wherein R27 is H.
 673. The method of any one of claims 25-671, wherein R27 is a halogen.
 674. The method of any one of claims 25-671, wherein R27 is hydroxy.
 675. The method of any one of claims 25-671, wherein R27 is amino.
 676. The method of any one of claims 25-671, wherein R27 is oxo.
 677. The method of any one of claims 25-671, wherein R27 is formyl.
 678. The method of any one of claims 25-671, wherein R27 is isocyano.
 679. The method of any one of claims 25-671, wherein R27 is carbamoyl.
 680. The method of any one of claims 25-671, wherein R27 is nitro.
 681. The method of any one of claims 25-671, wherein R27 is ethenyl.
 682. The method of any one of claims 25-671, wherein R27 is ethynyl.
 683. The method of any one of claims 25-671, wherein R27 is prop-1-enyl.
 684. The method of any one of claims 25-671, wherein R27 is propen-2-yl.
 685. The method of any one of claims 25-671, wherein R27 is prenyl.
 686. The method of any one of claims 25-671, wherein R27 is geranyl.
 687. The method of any one of claims 25-671, wherein R27 is hydroxy.
 688. The method of any one of claims 25-671, wherein R27 is methoxy.
 689. The method of any one of claims 25-671, wherein R27 is ethoxy.
 690. The method of any one of claims 25-671, wherein R27 is 2-propoxy.
 691. The method of any one of claims 25-671, wherein R27 is formyl.
 692. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted methyl.
 693. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted ethyl.
 694. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted propyl.
 695. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted butyl.
 696. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted pentyl.
 697. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted hexyl.
 698. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted heptyl.
 699. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted acetyl.
 700. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted propionyl.
 701. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted 2-oxo-propyl.
 702. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted butyryl.
 703. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted 3-oxo-butyl.
 704. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted phenyl.
 705. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted benzyl.
 706. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted phenylcarbonyl.
 707. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted 2-phenylethyl.
 708. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted 2-phenylethenyl.
 709. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 710. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 cycloalkyl.
 711. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 aryl.
 712. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylalkyl.
 713. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 714. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 715. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 716. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 717. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 718. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 719. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 720. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 721. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 722. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 723. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 724. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 725. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 726. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 727. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 728. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 729. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 730. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 731. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 732. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 733. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 734. The method of any one of claims 25-671, wherein R27 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 735. The method of any one of claims 20-734, wherein R3 is H.
 736. The method of any one of claims 20-734, wherein R3 is a halogen.
 737. The method of any one of claims 20-734, wherein R3 is hydroxy.
 738. The method of any one of claims 20-734, wherein R3 is amino.
 739. The method of any one of claims 20-734, wherein R3 is oxo.
 740. The method of any one of claims 20-734, wherein R3 is formyl.
 741. The method of any one of claims 20-734, wherein R3 is isocyano.
 742. The method of any one of claims 20-734, wherein R3 is carbamoyl.
 743. The method of any one of claims 20-734, wherein R3 is nitro.
 744. The method of any one of claims 20-734, wherein R3 is ethenyl.
 745. The method of any one of claims 20-734, wherein R3 is ethynyl.
 746. The method of any one of claims 20-734, wherein R3 is prop-1-enyl.
 747. The method of any one of claims 20-734, wherein R3 is propen-2-yl.
 748. The method of any one of claims 20-734, wherein R3 is prenyl.
 749. The method of any one of claims 20-734, wherein R3 is geranyl.
 750. The method of any one of claims 20-734, wherein R3 is methoxy.
 751. The method of any one of claims 20-734, wherein R3 is ethoxy.
 752. The method of any one of claims 20-734, wherein R3 is 2-propoxy.
 753. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted methyl.
 754. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted ethyl.
 755. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted propyl.
 756. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted butyl.
 757. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted pentyl.
 758. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted hexyl.
 759. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted heptyl.
 760. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted acetyl.
 761. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted propionyl.
 762. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted 2-oxo-propyl.
 763. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted butyryl.
 764. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted 3-oxo-butyl.
 765. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted phenyl.
 766. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted benzyl.
 767. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted phenylcarbonyl.
 768. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted 2-phenylethyl.
 769. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted 2-phenylethenyl.
 770. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 771. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 cycloalkyl.
 772. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 aryl.
 773. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylalkyl.
 774. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 775. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 776. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 777. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 778. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 779. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 780. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 781. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 782. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 783. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 784. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 785. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 786. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 787. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 788. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 789. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 790. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 791. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 792. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 793. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 794. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 795. The method of any one of claims 20-734, wherein R3 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 796. The method of any one of claims 20-795, wherein R5 is H.
 797. The method of any one of claims 20-795, wherein R5 is a halogen.
 798. The method of any one of claims 20-795, wherein R5 is hydroxy.
 799. The method of any one of claims 20-795, wherein R5 is amino.
 800. The method of any one of claims 20-795, wherein R5 is oxo.
 801. The method of any one of claims 20-795, wherein R5 is formyl.
 802. The method of any one of claims 20-795, wherein R5 is isocyano.
 803. The method of any one of claims 20-795, wherein R5 is carbamoyl.
 804. The method of any one of claims 20-795, wherein R5 is nitro.
 805. The method of any one of claims 20-795, wherein R5 is ethenyl.
 806. The method of any one of claims 20-795, wherein R5 is ethynyl.
 807. The method of any one of claims 20-795, wherein R5 is prop-1-enyl.
 808. The method of any one of claims 20-795, wherein R5 is propen-2-yl.
 809. The method of any one of claims 20-795, wherein R5 is prenyl.
 810. The method of any one of claims 20-795, wherein R5 is geranyl.
 811. The method of any one of claims 20-795, wherein R5 is methoxy.
 812. The method of any one of claims 20-795, wherein R5 is ethoxy.
 813. The method of any one of claims 20-795, wherein R5 is 2-propoxy.
 814. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted methyl.
 815. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted ethyl.
 816. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted propyl.
 817. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted butyl.
 818. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted pentyl.
 819. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted hexyl.
 820. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted heptyl.
 821. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted acetyl.
 822. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted propionyl.
 823. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted 2-oxo-propyl.
 824. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted butyryl.
 825. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted 3-oxo-butyl.
 826. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted phenyl.
 827. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted benzyl.
 828. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted phenylcarbonyl.
 829. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted 2-phenylethyl.
 830. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted 2-phenylethenyl.
 831. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 832. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 cycloalkyl.
 833. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 aryl.
 834. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylalkyl.
 835. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 836. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 837. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 838. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 839. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 840. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 841. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 842. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 843. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 844. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 845. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 846. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 847. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 848. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 849. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 850. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 851. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 852. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 853. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 854. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 855. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 856. The method of any one of claims 20-795, wherein R5 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 857. The method of any one of claims 20-856, wherein R7 is H.
 858. The method of any one of claims 20-856, wherein R7 is a halogen.
 859. The method of any one of claims 20-856, wherein R7 is hydroxy.
 860. The method of any one of claims 20-856, wherein R7 is amino.
 861. The method of any one of claims 20-856, wherein R7 is oxo.
 862. The method of any one of claims 20-856, wherein R7 is formyl.
 863. The method of any one of claims 20-856, wherein R7 is isocyano.
 864. The method of any one of claims 20-856, wherein R7 is carbamoyl.
 865. The method of any one of claims 20-856, wherein R7 is nitro.
 866. The method of any one of claims 20-856, wherein R7 is ethenyl.
 867. The method of any one of claims 20-856, wherein R7 is ethynyl.
 868. The method of any one of claims 20-856, wherein R7 is prop-1-enyl.
 869. The method of any one of claims 20-856, wherein R7 is propen-2-yl.
 870. The method of any one of claims 20-856, wherein R7 is prenyl.
 871. The method of any one of claims 20-856, wherein R7 is geranyl.
 872. The method of any one of claims 20-856, wherein R7 is methoxy.
 873. The method of any one of claims 20-856, wherein R7 is ethoxy.
 874. The method of any one of claims 20-856, wherein R7 is 2-propoxy.
 875. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted methyl.
 876. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted ethyl.
 877. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted propyl.
 878. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted butyl.
 879. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted pentyl.
 880. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted hexyl.
 881. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted heptyl.
 882. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted acetyl.
 883. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted propionyl.
 884. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted 2-oxo-propyl.
 885. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted butyryl.
 886. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted 3-oxo-butyl.
 887. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted phenyl.
 888. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted benzyl.
 889. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted phenylcarbonyl.
 890. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted 2-phenylethyl.
 891. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted 2-phenylethenyl.
 892. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 893. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 cycloalkyl.
 894. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 aryl.
 895. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylalkyl.
 896. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 897. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 898. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 899. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 900. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 901. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 902. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 903. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 904. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 905. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 906. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 907. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 908. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 909. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 910. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 911. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 912. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 913. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 914. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 915. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 916. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 917. The method of any one of claims 20-856, wherein R7 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 918. The method of any one of claims 20-917, wherein R9 is H.
 919. The method of any one of claims 20-917, wherein R9 is a halogen.
 920. The method of any one of claims 20-917, wherein R9 is hydroxy.
 921. The method of any one of claims 20-917, wherein R9 is amino.
 922. The method of any one of claims 20-917, wherein R9 is oxo.
 923. The method of any one of claims 20-917, wherein R9 is formyl.
 924. The method of any one of claims 20-917, wherein R9 is isocyano.
 925. The method of any one of claims 20-917, wherein R9 is carbamoyl.
 926. The method of any one of claims 20-917, wherein R9 is nitro.
 927. The method of any one of claims 20-917, wherein R9 is ethenyl.
 928. The method of any one of claims 20-917, wherein R9 is ethynyl.
 929. The method of any one of claims 20-917, wherein R9 is prop-1-enyl.
 930. The method of any one of claims 20-917, wherein R9 is propen-2-yl.
 931. The method of any one of claims 20-917, wherein R9 is prenyl.
 932. The method of any one of claims 20-917, wherein R9 is geranyl.
 933. The method of any one of claims 20-917, wherein R9 is methoxy.
 934. The method of any one of claims 20-917, wherein R9 is ethoxy.
 935. The method of any one of claims 20-917, wherein R9 is 2-propoxy.
 936. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted methyl.
 937. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted ethyl.
 938. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted propyl.
 939. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted butyl.
 940. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted pentyl.
 941. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted hexyl.
 942. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted heptyl.
 943. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted acetyl.
 944. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted propionyl.
 945. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted 2-oxo-propyl.
 946. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted butyryl.
 947. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted 3-oxo-butyl.
 948. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted phenyl.
 949. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted benzyl.
 950. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted phenylcarbonyl.
 951. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted 2-phenylethyl.
 952. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted 2-phenylethenyl.
 953. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 954. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 cycloalkyl.
 955. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 aryl.
 956. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylalkyl.
 957. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 958. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 959. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 960. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 961. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 962. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 963. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 964. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 965. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 966. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 967. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 968. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 969. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 970. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 971. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 972. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 973. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 974. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 975. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 976. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 977. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 978. The method of any one of claims 20-917, wherein R9 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 979. The method of any one of claims 20-978, wherein R11 is H.
 980. The method of any one of claims 20-978, wherein R11 is a halogen.
 981. The method of any one of claims 20-978, wherein R11 is hydroxy.
 982. The method of any one of claims 20-978, wherein R11 is amino.
 983. The method of any one of claims 20-978, wherein R11 is oxo.
 984. The method of any one of claims 20-978, wherein R11 is formyl.
 985. The method of any one of claims 20-978, wherein R11 is isocyano.
 986. The method of any one of claims 20-978, wherein R11 is carbamoyl.
 987. The method of any one of claims 20-978, wherein R11 is nitro.
 988. The method of any one of claims 20-978, wherein R11 is ethenyl.
 989. The method of any one of claims 20-978, wherein R11 is ethynyl.
 990. The method of any one of claims 20-978, wherein R11 is prop-1-enyl.
 991. The method of any one of claims 20-978, wherein R11 is propen-2-yl.
 992. The method of any one of claims 20-978, wherein R11 is prenyl.
 993. The method of any one of claims 20-978, wherein R11 is geranyl.
 994. The method of any one of claims 20-978, wherein R11 is methoxy.
 995. The method of any one of claims 20-978, wherein R11 is ethoxy.
 996. The method of any one of claims 20-978, wherein R11 is 2-propoxy.
 997. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted methyl.
 998. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted ethyl.
 999. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted propyl.
 1000. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted butyl.
 1001. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted pentyl.
 1002. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted hexyl.
 1003. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted heptyl.
 1004. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted acetyl.
 1005. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted propionyl.
 1006. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted 2-oxo-propyl.
 1007. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted butyryl.
 1008. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted 3-oxo-butyl.
 1009. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted phenyl.
 1010. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted benzyl.
 1011. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted phenylcarbonyl.
 1012. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted 2-phenylethyl.
 1013. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted 2-phenylethenyl.
 1014. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted 3-phenylprop-2-enonyl.
 1015. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 cycloalkyl.
 1016. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 aryl.
 1017. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylalkyl.
 1018. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylcarbonyl.
 1019. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 1020. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylcarbonylamino.
 1021. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 1022. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylcarbamoyl.
 1023. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 1024. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 1025. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 1026. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 1027. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 1028. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyl.
 1029. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylidene.
 1030. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy.
 1031. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanyl.
 1032. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylamino.
 1033. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyl.
 1034. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonyloxy.
 1035. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylsulfanyl.
 1036. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbonylamino.
 1037. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxycarbonyl.
 1038. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylsulfanylcarbonyl.
 1039. The method of any one of claims 20-978, wherein R11 is a substituted or unsubstituted, straight-or-branched C1-C12 alkylcarbamoyl.
 1040. The method of any one of claims 20-1039, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a halogen.
 1041. The method of any one of claims 20-1040, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with hydroxy.
 1042. The method of any one of claims 20-1041, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with methoxy.
 1043. The method of any one of claims 20-1042, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with ethoxy.
 1044. The method of any one of claims 20-1043, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with propoxy.
 1045. The method of any one of claims 20-1044, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with amino.
 1046. The method of any one of claims 20-1045, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with formyl.
 1047. The method of any one of claims 20-1046, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with isocyano.
 1048. The method of any one of claims 20-1047, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with carbamoyl.
 1049. The method of any one of claims 20-1048, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with nitro.
 1050. The method of any one of claims 20-1049, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted methyl.
 1051. The method of any one of claims 20-1050, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted ethyl.
 1052. The method of any one of claims 20-1051, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted propyl.
 1053. The method of any one of claims 20-1052, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted butyl.
 1054. The method of any one of claims 20-1053, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted pentyl.
 1055. The method of any one of claims 20-1054, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted hexyl.
 1056. The method of any one of claims 20-1055, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted heptyl.
 1057. The method of any one of claims 20-1056, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted octanyl.
 1058. The method of any one of claims 20-1057, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted nonanyl.
 1059. The method of any one of claims 20-1058, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted decanyl.
 1060. The method of any one of claims 20-1059, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted undecanyl.
 1061. The method of any one of claims 20-1060, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted dodecanyl.
 1062. The method of any one of claims 20-1061, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted cyclohexyl.
 1063. The method of any one of claims 20-1062, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted phenyl.
 1064. The method of any one of claims 20-1063, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted benzyl.
 1065. The method of any one of claims 20-1064, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 cycloalkyl.
 1066. The method of any one of claims 20-1065, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 aryl.
 1067. The method of any one of claims 20-1066, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylalkyl.
 1068. The method of any one of claims 20-1067, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylcarbonyl.
 1069. The method of any one of claims 20-1068, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylcarbonyloxy.
 1070. The method of any one of claims 20-1069, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylcarbonylamino.
 1071. The method of any one of claims 20-1070, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 aryloxycarbonyl.
 1072. The method of any one of claims 20-1071, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylcarbamoyl.
 1073. The method of any one of claims 20-1072, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylalkylcarbonyl.
 1074. The method of any one of claims 20-1073, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylalkylcarbonyloxy.
 1075. The method of any one of claims 20-1074, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylalkylcarbonylamino.
 1076. The method of any one of claims 20-1075, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylalkyloxycarbonyl.
 1077. The method of any one of claims 20-1076, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C3-C10 arylalkylcarbamoyl.
 1078. The method of any one of claims 20-1077, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkyl.
 1079. The method of any one of claims 20-1078, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkylidene.
 1080. The method of any one of claims 20-1079, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkyloxy.
 1081. The method of any one of claims 20-1080, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkylsulfanyl.
 1082. The method of any one of claims 20-1081, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkylamino.
 1083. The method of any one of claims 20-1082, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkylcarbonyl.
 1084. The method of any one of claims 20-1083, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkylcarbonyloxy.
 1085. The method of any one of claims 20-1084, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkylcarbonylsulfanyl.
 1086. The method of any one of claims 20-1085, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkylcarbonylamino.
 1087. The method of any one of claims 20-1086, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkyloxycarbonyl.
 1088. The method of any one of claims 20-1087, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkylsulfanylcarbonyl.
 1089. The method of any one of claims 20-1088, wherein a hydrogen atom of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a substituted or unsubstituted C1-C12 alkylcarbamoyl.
 1090. The method of any one of claims 20-1089, wherein a double bond of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with two hydrogen atoms.
 1091. The method of any one of claims 20-1090, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a double bond.
 1092. The method of any one of claims 20-1091, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with oxo.
 1093. The method of any one of claims 20-1092, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with methylidene.
 1094. The method of any one of claims 20-1093, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with methylene such that the substitution of the two hydrogen atoms forms a cycle that consists of 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 atoms.
 1095. The method of any one of claims 20-1094, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with epoxy such that the substitution of the two hydrogen atoms forms a cycle that consists of 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 atoms.
 1096. The method of any one of claims 20-1095, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a straight C1-C12 alkyl such that the substitution of the two hydrogen atoms forms a cycle that consists of 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 atoms.
 1097. The method of any one of claims 20-1096, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a branched C1-C12 alkyl such that the substitution of the two hydrogen atoms forms a cycle that consists of 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 atoms.
 1098. The method of any one of claims 20-1097, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with methylenedioxy.
 1099. The method of any one of claims 20-1098, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a straight C1-C12 alkylidene.
 1100. The method of any one of claims 20-1099, wherein two hydrogen atoms of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a branched C1-C12 alkylidene.
 1101. The method of any one of claims 20-1100, wherein a methylene bridge of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with an oxygen atom.
 1102. The method of any one of claims 20-1101, wherein a methylene bridge of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a sulfur atom.
 1103. The method of any one of claims 20-1102, wherein a methylene bridge of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a sulfinyl.
 1104. The method of any one of claims 20-1103, wherein a methylene bridge of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a sulfonyl.
 1105. The method of any one of claims 20-1104, wherein a methylene bridge of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a protonated nitrogen atom.
 1106. The method of any one of claims 20-1105, wherein a methylene bridge of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a straight C1-C12 alkylamino.
 1107. The method of any one of claims 20-1106, wherein a methylene bridge of exactly one of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted with a branched C1-C12 alkylamino.
 1108. The method of any one of claims 20-1107, wherein exactly 1 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted.
 1109. The method of any one of claims 20-1107, wherein exactly 1 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted exactly 1 time.
 1110. The method of any one of claims 20-1107, wherein exactly 1 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted exactly 2 times.
 1111. The method of any one of claims 20-1107, wherein exactly 1 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 is substituted exactly 3 times.
 1112. The method of any one of claims 20-1107, wherein exactly 2 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 are substituted.
 1113. The method of any one of claims 20-1107, wherein exactly 2 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 are substituted exactly 1 time each.
 1114. The method of any one of claims 20-1107, wherein exactly 2 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 are substituted no greater than 2 times each.
 1115. The method of any one of claims 20-1107, wherein exactly 2 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 are substituted no greater than 3 times each.
 1116. The method of any one of claims 20-1107, wherein exactly 3 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 are substituted.
 1117. The method of any one of claims 20-1107, wherein exactly 3 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 are substituted exactly 1 time each.
 1118. The method of any one of claims 20-1107, wherein exactly 3 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 are substituted no greater than 2 times each.
 1119. The method of any one of claims 20-1107, wherein exactly 3 of R3, R4, R5, R7, R9, R11, R21, R23, R25, R27, R29, R33, R34, R35, R36, R37, and R39 are substituted no greater than 3 times each.
 1120. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 16 carbon atoms.
 1121. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 17 carbon atoms.
 1122. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 18 carbon atoms.
 1123. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 19 carbon atoms.
 1124. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 20 carbon atoms.
 1125. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 21 carbon atoms.
 1126. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 22 carbon atoms.
 1127. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 23 carbon atoms.
 1128. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 24 carbon atoms.
 1129. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 25 carbon atoms.
 1130. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 26 carbon atoms.
 1131. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 27 carbon atoms.
 1132. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 28 carbon atoms.
 1133. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 29 carbon atoms.
 1134. The method of any one of claims 20-1119, wherein each R group is selected such that the anion comprises exactly 30 carbon atoms.
 1135. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 16 hydrogen atoms.
 1136. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 17 hydrogen atoms.
 1137. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 18 hydrogen atoms.
 1138. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 19 hydrogen atoms.
 1139. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 20 hydrogen atoms.
 1140. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 21 hydrogen atoms.
 1141. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 22 hydrogen atoms.
 1142. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 23 hydrogen atoms.
 1143. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 24 hydrogen atoms.
 1144. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 25 hydrogen atoms.
 1145. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 26 hydrogen atoms.
 1146. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 27 hydrogen atoms.
 1147. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 28 hydrogen atoms.
 1148. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 29 hydrogen atoms.
 1149. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 30 hydrogen atoms.
 1150. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 31 hydrogen atoms.
 1151. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 32 hydrogen atoms.
 1152. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 33 hydrogen atoms.
 1153. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 34 hydrogen atoms.
 1154. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 35 hydrogen atoms.
 1155. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 36 hydrogen atoms.
 1156. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 37 hydrogen atoms.
 1157. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 38 hydrogen atoms.
 1158. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 39 hydrogen atoms.
 1159. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 40 hydrogen atoms.
 1160. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 41 hydrogen atoms.
 1161. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 42 hydrogen atoms.
 1162. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 43 hydrogen atoms.
 1163. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 44 hydrogen atoms.
 1164. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 45 hydrogen atoms.
 1165. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 46 hydrogen atoms.
 1166. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 47 hydrogen atoms.
 1167. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 48 hydrogen atoms.
 1168. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 49 hydrogen atoms.
 1169. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 50 hydrogen atoms.
 1170. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 51 hydrogen atoms.
 1171. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 52 hydrogen atoms.
 1172. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 53 hydrogen atoms.
 1173. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 54 hydrogen atoms.
 1174. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 55 hydrogen atoms.
 1175. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 56 hydrogen atoms.
 1176. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 57 hydrogen atoms.
 1177. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 58 hydrogen atoms.
 1178. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 59 hydrogen atoms.
 1179. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 60 hydrogen atoms.
 1180. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 61 hydrogen atoms.
 1181. The method of any one of claims 20-1134, wherein each R group is selected such that the anion comprises exactly 62 hydrogen atoms.
 1182. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 1 oxygen atom.
 1183. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 2 oxygen atoms.
 1184. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 3 oxygen atoms.
 1185. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 4 oxygen atoms.
 1186. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 5 oxygen atoms.
 1187. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 6 oxygen atoms.
 1188. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 7 oxygen atoms.
 1189. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 8 oxygen atoms.
 1190. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 9 oxygen atoms.
 1191. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 10 oxygen atoms.
 1192. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 11 oxygen atoms.
 1193. The method of any one of claims 20-1181, wherein each R group is selected such that the anion comprises exactly 12 oxygen atoms.
 1194. The method of any one of claims 20-1193, wherein each R group is selected such that the anion comprises exactly 0 sulfur atoms.
 1195. The method of any one of claims 20-1193, wherein each R group is selected such that the anion comprises exactly 1 sulfur atom.
 1196. The method of any one of claims 20-1195, wherein each R group is selected such that the anion comprises exactly 0 nitrogen atoms.
 1197. The method of any one of claims 20-1195, wherein each R group is selected such that the anion comprises exactly 1 nitrogen atom.
 1198. The method of any one of claims 20-1197, wherein each R group is selected such that the anion comprises exactly 0 halogen atoms.
 1199. The method of any one of claims 20-1197, wherein each R group is selected such that the anion comprises exactly 1 halogen atom.
 1200. The method of any one of claims 20-1197, wherein each R group is selected such that the anion comprises exactly 2 halogen atoms.
 1201. The method of any one of claims 20-1197, wherein each R group is selected such that the anion comprises exactly 3 halogen atoms.
 1202. The method of any one of claims 20-1201, wherein each R group is selected such that the anion comprises no greater than 6 total combined sulfur, nitrogen, and halogen atoms.
 1203. The method of any one of claims 20-1201, wherein each R group is selected such that the anion comprises no greater than 5 total combined sulfur, nitrogen, and halogen atoms.
 1204. The method of any one of claims 20-1201, wherein each R group is selected such that the anion comprises no greater than 4 total combined sulfur, nitrogen, and halogen atoms.
 1205. The method of any one of claims 20-1201, wherein each R group is selected such that the anion comprises no greater than 3 total combined sulfur, nitrogen, and halogen atoms.
 1206. The method of any one of claims 20-1200, wherein each R group is selected such that the anion comprises no greater than 2 total combined sulfur, nitrogen, and halogen atoms.
 1207. The method of any one of claims 20-1199, wherein each R group is selected such that the anion comprises no greater than 1 total combined sulfur, nitrogen, and halogen atoms.
 1208. The method of any one of claims 21-1207, wherein C3-C10 refers to an R group that comprises exactly 3, 4, 5, 6, 7, 8, 9, or 10 carbon atoms.
 1209. The method of any one of claims 21-1208, wherein C3-C10 refers to an R group that is a C3 R group that comprises exactly 3 carbon atoms.
 1210. The method of any one of claims 21-1208, wherein C3-C10 refers to an R group that is a C4 R group that comprises exactly 4 carbon atoms.
 1211. The method of any one of claims 21-1208, wherein C3-C10 refers to an R group that is a C5 R group that comprises exactly 5 carbon atoms.
 1212. The method of any one of claims 21-1208, wherein C3-C10 refers to an R group that is a C6 R group that comprises exactly 6 carbon atoms.
 1213. The method of any one of claims 21-1208, wherein C3-C10 refers to an R group that is a C7 R group that comprises exactly 7 carbon atoms.
 1214. The method of any one of claims 21-1208, wherein C3-C10 refers to an R group that is a C8 R group that comprises exactly 8 carbon atoms.
 1215. The method of any one of claims 21-1208, wherein C3-C10 refers to an R group that is a C9 R group that comprises exactly 9 carbon atoms.
 1216. The method of any one of claims 21-1208, wherein C3-C10 refers to an R group that is a C10 R group that comprises exactly 10 carbon atoms.
 1217. The method of any one of claims 21-1216, wherein C1-C12 refers to an R group that comprises exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms.
 1218. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C1 R group that comprises exactly 1 carbon atom.
 1219. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C2 R group that comprises exactly 2 carbon atoms.
 1220. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C3 R group that comprises exactly 3 carbon atoms.
 1221. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C4 R group that comprises exactly 4 carbon atoms.
 1222. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C5 R group that comprises exactly 5 carbon atoms.
 1223. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C6 R group that comprises exactly 6 carbon atoms.
 1224. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C7 R group that comprises exactly 7 carbon atoms.
 1225. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C8 R group that comprises exactly 8 carbon atoms.
 1226. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C9 R group that comprises exactly 9 carbon atoms.
 1227. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C10 R group that comprises exactly 10 carbon atoms.
 1228. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C11 R group that comprises exactly 11 carbon atoms.
 1229. The method of any one of claims 21-1217, wherein C1-C12 refers to an R group that is a C12 R group that comprises exactly 12 carbon atoms.
 1230. The method of any one of claims 20-1229, wherein the anion has the general structure I or II; and R3 is H, F, Cl, Br, or I.
 1231. The method of any one of claims 20-1230, wherein the anion has the general structure I or II; R3 is H.
 1232. The method of any one of claims 20-1229, wherein the anion has the general structure III; and R3 is methyl, hydroxymethyl, fluoromethyl, 3-hydroxypropyl, 3-hydroxyprop-1-enyl, or 3-hydroxyprop-1-ynyl.
 1233. The method of any one of claims 20-1229, wherein the anion has the general structure III; and R3 is methyl.
 1234. The method of any one of claims 20-1233, wherein R4 is methyl.
 1235. The method of any one of claims 20-1234, wherein either (i) the anion has the general structure I or II and R5 is, or (ii) the anion has the general structure III and R25 is: methyl; ethyl; propyl; butyl; pentyl; hexyl; heptyl; octyl; nonyl; decyl; undecyl; dodecyl; prop-2-yl; but-2-yl; pent-2-yl; hex-2-yl; hept-2-yl; octan-2-yl; nonan-2-yl; dec-2-yl; undec-2-yl; dodec-2-yl; 2-methylpropyl; 2-methylbutyl; 2-methylpentyl; 2-methylhexyl; 2-methylheptyl; 2-methyloctyl; 2-methylnonyl; 2-methyldecyl; 2-methylundecyl; 2-methylprop-2-yl; 2-methylbut-2-yl; 2-methylpent-2-yl; 2-methylhex-2-yl; 2-methylhept-2-yl; 2-methyloct-2-yl; 2-methylnonan-2-yl; 2-methyldec-2-yl; 2-methylundec-2-yl; 3-methylbut-2-yl; 3-methylpent-2-yl; 3-methylhex-2-yl; 3-methylhept-2-yl; 3-methyloct-2-yl; 3-methylnonan-2-yl; 3-methyldec-2-yl; 3-methylundec-2-yl; 2,3-dimethylbut-2-yl; 2,3-dimethylpent-2-yl; 2,3-dimethylhex-2-yl; 2,3-dimethylhept-2-yl; 2,3-dimethyloct-2-yl; 2,3-dimethylnonan-2-yl; 2,3-dimethyldec-2-yl; cyclopropyl; 1-methylcyclopropyl; 1-ethylcyclopropyl; 1-propylcyclopropyl; 1-butylcyclopropyl; 1-pentylcyclopropyl; 1-hexylcyclopropyl; 1-heptylcyclopropyl; 1-octylcyclopropyl; 1-nonylcyclopropyl; cyclobutyl; 1-methylcyclobutyl; 1-ethylcyclobutyl; 1-propylcyclobutyl; 1-butylcyclobutyl; 1-pentylcyclobutyl; 1-hexylcyclobutyl; 1-heptylcyclobutyl; 1-octylcyclobutyl; cyclopentyl; 1-methylcyclopentyl; 1-ethylcyclopentyl; 1-propylcyclopentyl; 1-butylcyclopentyl; 1-pentylcyclopentyl; 1-hexylcyclopentyl; 1-heptylcyclopentyl; cyclohexyl; 1-methylcyclohexyl; 1-ethylcyclohexyl; 1-propylcyclohexyl; 1-butylcyclohexyl; 1-pentylcyclohexyl; 1-hexylcyclohexyl; ethenyl; prop-1-enyl; but-1-enyl; pent-1-enyl; hex-1-enyl; hept-1-enyl; oct-1-enyl; nonan-1-enyl; dec-1-enyl; undec-1-enyl; dodec-1-enyl; ethynyl; prop-1-ynyl; but-1-ynyl; pent-1-ynyl; hex-1-ynyl; hept-1-ynyl; oct-1-ynyl; nonan-1-ynyl; dec-1-ynyl; undec-1-ynyl; dodec-1-ynyl; 2-phenylethyl; 2-phenylprop-2-yl; adamant-1-yl; adamant-2-yl; 6-fluorohex-2-enyl; 6-fluorohex-2-ynyl; 2-methyl-6-fluorohex-2-yl; 6-chlorohex-2-enyl; 6-chlorohex-2-ynyl; 2-methyl-6-chlorohex-2-yl; 6-bromohex-2-enyl; 6-bromohex-2-ynyl; 2-methyl-6-bromohex-2-yl; 6-iodohex-2-enyl; 6-iodohex-2-ynyl; or 2-methyl-6-iodohex-2-yl.
 1236. The method of any one of claims 20-1235, wherein the anion has the general structure I or II; and R5 is propyl, butyl, pentyl, hexyl, heptyl, 2-methyloct-2-yl, or 2-phenylethyl.
 1237. The method of any one of claims 20-1236, wherein the anion has the general structure I or II; and R5 is pentyl.
 1238. The method of any one of claims 20-1235, wherein the anion has the general structure III; and R5 is propyl, butyl, pentyl, hexyl, heptyl, 2-methyloct-2-yl, or 2-phenylethyl.
 1239. The method of any one of claims 20-1235, wherein the anion has the general structure III; and R5 is pentyl.
 1240. The method of any one of claims 20-1239, wherein R7 is H.
 1241. The method of any one of claims 20-1240, wherein R8 is H.
 1242. The method of any one of claims 20-1241, wherein R9 is H; F; Cl; Br; I; hydroxy; methoxy; ethoxy; 2-propoxy; a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy; or a substituted or unsubstituted C3-C10 alkylcarbonyloxy, methylcarbonyloxy, or ethylcarbonyloxy.
 1243. The method of any one of claims 20-1242, wherein R9 is hydroxy.
 1244. The method of any one of claims 20-1243, wherein R11 is prenyl, geranyl, or a substituted C3-C10 cycloalkyl.
 1245. The method of any one of claims 20-1244, wherein R11 is a substituted C3-C10 cycloalkyl.
 1246. The method of any one of claims 20-1245, wherein R11 is a substituted C3-C10 cycloalkyl; and substituted refers to at least one of, in any order and without limitation, the substitution of two hydrogen atoms with a double bond; and the substitution of a hydrogen atom with a formyl or a substituted orunsubstituted, straight-or-branched C1-C12 alkyl, alkylidene, alkylcarbonyl, or alkyloxycarbonyl.
 1247. The method of any one of claims 20-1246, wherein R11 is a substituted C3-C10 cycloalkyl; and substituted refers to at least one of, in any order and without limitation, the substitution of two hydrogen atoms with a double bond, oxo, or methylidene; and the substitution of a hydrogen atom with a halogen; or a substituted or unsubstituted methyl, ethyl, or propyl.
 1248. The method of any one of claims 20-1247, wherein R11 is a substituted C3-C10 cycloalkyl; and substituted refers to at least one of, in any order and without limitation, the substitution of two hydrogen atoms with a double bond; and the substitution of a hydrogen atom with a substituted or unsubstituted methyl, ethyl, or propyl.
 1249. The method of claim 1248, wherein the anion is 3-hydroxy-2-(6-isopropenyl-3-methylcyclohex-2-enyl)-5-pentylphenolate.
 1250. The method of any one of claims 20-1244, wherein R11 is geranyl.
 1251. The method of any one of claims 20-1250, wherein the anion has the general structure II; and R21 is 2-propyl or 2-propenyl.
 1252. The method of any one of claims 20-1250, wherein the anion has the general structure III; and R21 is oxide.
 1253. The method of any one of claims 20-1252, wherein R23 is H.
 1254. The method of any one of claims 20-1253, wherein the anion has the general structure II; and R25 is H, F, Cl, Br, or I.
 1255. The method of any one of claims 20-1254, wherein the anion has the general structure II; and R27 is H, a halogen, hydroxy, oxo, formyl, isocyano, or a substituted or unsubstituted, straight-or-branched C1-C12 alkyl, alkylidene, alkylcarbonyl, or alkyloxycarbonyl.
 1256. The method of any one of claims 20-1255, wherein the anion has the general structure II; and R27 is methyl, hydroxymethyl, or oxo.
 1257. The method of any one of claims 20-1256, wherein the anion has the general structure II; and R27 is methyl.
 1258. The method of any one of claims 20-1253, wherein the anion has the general structure III; and R27 is H; F; Cl; Br; I; hydroxy; methoxy; ethoxy; 2-propoxy; a substituted or unsubstituted, straight-or-branched C1-C12 alkyloxy; or a substituted or unsubstituted C3-C10 alkylcarbonyloxy, methylcarbonyloxy, or ethylcarbonyloxy.
 1259. The method of any one of claims 20-1253, wherein the anion has the general structure III; and R27 is hydroxy.
 1260. The method of any one of claims 20-1259, wherein R29 is H.
 1261. The method of any one of claims 20-1260, wherein R33 is H.
 1262. The method of any one of claims 20-1261, wherein R34 is H.
 1263. The method of any one of claims 20-1262, wherein R35 is H.
 1264. The method of any one of claims 20-1263, wherein R36 is H.
 1265. The method of any one of claims 20-1264, wherein R37 is H, a halogen, hydroxy, oxo, formyl, isocyano, or a substituted or unsubstituted, straight-or-branched C1-C12 alkyl, alkylidene, alkylcarbonyl, or alkyloxycarbonyl.
 1266. The method of any one of claims 20-1265, wherein R37 is methyl, hydroxymethyl, or oxo.
 1267. The method of any one of claims 20-1266, wherein R37 is methyl.
 1268. The method of any one of claims 20-1267, wherein R39 is H, F, Cl, Br, or I.
 1269. The method of any one of claims 20-1268, wherein R39 is H.
 1270. The method of any one of claims 16-1269, wherein the anion is 2-geranyl-3-hydroxy-5-pentylphenolate.
 1271. The method of any one of claims 16-1269, wherein the anion is 3-hydroxy-2-(6-isopropenyl-3-methylcyclohex-2-enyl)-5-pentylphenolate.
 1272. The method of any one of claims 16-1269, wherein the anion is 3-hydroxy-2-(6-isopropenyl-3-methylcyclohex-3-enyl)-5-pentylphenolate.
 1273. The method of any one of claims 16-1269, wherein the anion is 6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromene-1-oxide.
 1274. The method of any one of claims 16-1269, wherein the anion is 6,6,9-trimethyl-3-pentyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromene-1-oxide.
 1275. The method of any one of claims 16-1269, wherein the anion is 6,6,9-trimethyl-3-pentyl-6H-benzo[c]chromene-1-oxide.
 1276. The method of any one of claims 16-1269, wherein the anion is 5-alkyl-2-geranyl-3-hydroxyphenolate.
 1277. The method of any one of claims 16-1269, wherein the anion is 5-alkyl-3-hydroxy-2-(6-isopropenyl-3-methylcyclohex-2-enyl)phenolate.
 1278. The method of any one of claims 16-1269, wherein the anion is 5-alkyl-3-hydroxy-2-(6-isopropenyl-3-methylcyclohex-3-enyl)phenolate.
 1279. The method of any one of claims 16-1269, wherein the anion is 3-alkyl-6,6,9-trimethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromene-1-oxide.
 1280. The method of any one of claims 16-1269, wherein the anion is 3-alkyl-6,6,9-trimethyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromene-1-oxide.
 1281. The method of any one of claims 16-1269, wherein the anion is 3-alkyl-6,6,9-trimethyl-6H-benzo[c]chromen-1-oxide.
 1282. The method of any one of claims 16-1269, wherein the anion is 5-alkyl-2-geranyl-3-hydroxyphenolate.
 1283. The method of any one of claims 16-1269, wherein the anion is 3-alkyl-6,6-dimethyl-9-oxo-6,6a,7,8,10,10a-hexahydro-9H-benzo[c]chromen-1-oxide.
 1284. The method of any one of claims 16-1269, wherein the anion is 3-alkyl-9-(hydroxymethyl)-6,6-dimethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-oxide.
 1285. The method of any one of claims 16-1269, wherein the anion is 3-alkyl-9-(hydroxymethyl)-6,6-dimethyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromen-1-oxide.
 1286. The method of any one of claims 16-1269, wherein the anion is 7-alkyl-2-methyl-2-(4-methylpent-3-enyl)-2H-1-benzopyran-5-oxide.
 1287. The method of any one of claims 16-1269, wherein the anion is 3-alkyl-6,6,9-trimethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-oxide.
 1288. The method of any one of claims 16-1269, wherein the anion is 3-alkyl-6,6,9-trimethyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromen-1-oxide.
 1289. The method of any one of claims 16-1269, wherein the anion is 5-alkyl-2-(6-isopropenyl-3-methylcyclohex-2-enyl)-3-hydroxyphenolate.
 1290. The method of any one of claims 16-1269, wherein the anion is 5-alkyl-2-(6-isopropenyl-3-methylcyclohex-3-enyl)-3-hydroxyphenolate.
 1291. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched, saturated-or-unsaturated C1-C12 hydrocarbon group that is optionally substituted with one or more of hydroxy, cyano, oxa, phenyl, a cycloalkyl, and 1, 2, or 3 halogens.
 1292. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched alkyl, alkenyl, or alkynyl group comprising exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms, which is optionally substituted with one or more of hydroxy, cyano, oxa, phenyl, a cycloalkyl, and 1, 2, or 3 halogens.
 1293. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched, saturated-or-unsaturated C1-C12 hydrocarbon group that is substituted with one or more of hydroxy group(s) such that a one or more hydrogen atom(s) of the hydrocarbon group are substituted with one or more hydroxy group(s).
 1294. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched alkyl, alkenyl, or alkynyl group comprising exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms that is substituted with one or more hydroxy group(s) such that a one or more hydrogen atom(s) of the hydrocarbon group are substituted with one or more hydroxy group(s).
 1295. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched, saturated-or-unsaturated C1-C12 hydrocarbon group that is substituted with a cyano group such that a hydrogen atom of the hydrocarbon group is substituted with the cyano group.
 1296. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched alkyl, alkenyl, or alkynyl group comprising exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms that is substituted with a cyano group such that a hydrogen atom of the hydrocarbon group is substituted with the cyano group.
 1297. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched, saturated-or-unsaturated C1-C12 hydrocarbon group that is substituted with a phenyl group such that a hydrogen atom of the hydrocarbon group is substituted with the phenyl group.
 1298. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched alkyl, alkenyl, or alkynyl group comprising exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms that is substituted with a phenyl group such that a hydrogen atom of the hydrocarbon group is substituted with the phenyl group.
 1299. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched, saturated-or-unsaturated C1-C12 hydrocarbon group that is substituted with 1, 2, or 3 halogens such that 1, 2, or 3 hydrogen atom(s) of the hydrocarbon group are substituted with 1, 2, or 3 halogens.
 1300. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched alkyl, alkenyl, or alkynyl group comprising exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms that is substituted with 1, 2, or 3 halogens such that 1, 2, or 3 hydrogen atom(s) of the hydrocarbon group are substituted with 1, 2, or 3 halogens.
 1301. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched, saturated-or-unsaturated C1-C12 hydrocarbon group that is substituted with an oxa group such that a carbon atom of the hydrocarbon group is substituted with an oxygen atom.
 1302. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched alkyl, alkenyl, or alkynyl group comprising exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms that is substituted with an oxa group such that a carbon atom of the hydrocarbon group is substituted with an oxygen atom.
 1303. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched, saturated-or-unsaturated C1-C12 hydrocarbon group that is substituted with a cycloalkyl group such that a hydrogen atom of the hydrocarbon group is substituted with the cycloalkyl group.
 1304. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched alkyl, alkenyl, or alkynyl group comprising exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms that is substituted with a cycloalkyl group such that a hydrogen atom of the hydrocarbon group is substituted with the cycloalkyl group.
 1305. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched, saturated-or-unsaturated C1-C12 hydrocarbon group that is substituted with a cycloalkyl group such that two hydrogen atoms of the hydrocarbon group are substituted with the cycloalkyl group, and the cycloalkyl group comprises one or more carbon atoms of the hydrocarbon group.
 1306. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched alkyl, alkenyl, or alkynyl group comprising exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms that is substituted with a cycloalkyl group such that two hydrogen atoms of the hydrocarbon group are substituted with the cycloalkyl group, and the cycloalkyl group comprises one or more carbon atoms of the hydrocarbon group.
 1307. The method of any one of claims 1291-1306, wherein cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or adamantyl.
 1308. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched, saturated-or-unsaturated C1-C12 hydrocarbon group that is not further substituted.
 1309. The method of any one of claims 1276-1290, wherein alkyl is a straight-or-branched alkyl, alkenyl, or alkynyl group comprising exactly 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms, which is not further substituted.
 1310. The method of any one of claims 1276-1290, wherein alkyl is absent; methyl; ethyl; propyl; butyl; pentyl; hexyl; heptyl; octyl; nonyl; decyl; undecyl; dodecyl; prop-2-yl; but-2-yl; pent-2-yl; hex-2-yl; hept-2-yl; octan-2-yl; nonan-2-yl; dec-2-yl; undec-2-yl; dodec-2-yl; 2-methylpropyl; 2-methylbutyl; 2-methylpentyl; 2-methylhexyl; 2-methylheptyl; 2-methyloctyl; 2-methylnonyl; 2-methyldecyl; 2-methylundecyl; 2-methylprop-2-yl; 2-methylbut-2-yl; 2-methylpent-2-yl; 2-methylhex-2-yl; 2-methylhept-2-yl; 2-methyloct-2-yl; 2-methylnonan-2-yl; 2-methyldec-2-yl; 2-methylundec-2-yl; 3-methylbut-2-yl; 3-methylpent-2-yl; 3-methylhex-2-yl; 3-methylhept-2-yl; 3-methyloct-2-yl; 3-methylnonan-2-yl; 3-methyldec-2-yl; 3-methylundec-2-yl; 2,3-dimethylbut-2-yl; 2,3-dimethylpent-2-yl; 2,3-dimethylhex-2-yl; 2,3-dimethylhept-2-yl; 2,3-dimethyloct-2-yl; 2,3-dimethylnonan-2-yl; 2,3-dimethyldec-2-yl; cyclopropyl; 1-methylcyclopropyl; 1-ethylcyclopropyl; 1-propylcyclopropyl; 1-butylcyclopropyl; 1-pentylcyclopropyl; 1-hexylcyclopropyl; 1-heptylcyclopropyl; 1-octylcyclopropyl; 1-nonylcyclopropyl; cyclobutyl; 1-methylcyclobutyl; 1-ethylcyclobutyl; 1-propylcyclobutyl; 1-butylcyclobutyl; 1-pentylcyclobutyl; 1-hexylcyclobutyl; 1-heptylcyclobutyl; 1-octylcyclobutyl; cyclopentyl; 1-methylcyclopentyl; 1-ethylcyclopentyl; 1-propylcyclopentyl; 1-butylcyclopentyl; 1-pentylcyclopentyl; 1-hexylcyclopentyl; 1-heptylcyclopentyl; cyclohexyl; 1-methylcyclohexyl; 1-ethylcyclohexyl; 1-propylcyclohexyl; 1-butylcyclohexyl; 1-pentylcyclohexyl; 1-hexylcyclohexyl; ethenyl; prop-1-enyl; but-1-enyl; pent-1-enyl; hex-1-enyl; hept-1-enyl; oct-1-enyl; nonan-1-enyl; dec-1-enyl; undec-1-enyl; dodec-1-enyl; ethynyl; prop-1-ynyl; but-1-ynyl; pent-1-ynyl; hex-1-ynyl; hept-1-ynyl; oct-1-ynyl; nonan-1-ynyl; dec-1-ynyl; undec-1-ynyl; dodec-1-ynyl; 2-phenylethyl; 2-phenylprop-2-yl; adamant-1-yl; adamant-2-yl; 6-fluorohex-2-enyl; 6-fluorohex-2-ynyl; 2-methyl-6-fluorohex-2-yl; 6-chlorohex-2-enyl; 6-chlorohex-2-ynyl; 2-methyl-6-chlorohex-2-yl; 6-bromohex-2-enyl; 6-bromohex-2-ynyl; 2-methyl-6-bromohex-2-yl; 6-iodohex-2-enyl; 6-iodohex-2-ynyl; or 2-methyl-6-iodohex-2-yl.
 1311. The method of any one of claims 1276-1290, wherein alkyl is methyl.
 1312. The method of any one of claims 1276-1290, wherein alkyl is ethyl.
 1313. The method of any one of claims 1276-1290, wherein alkyl is propyl.
 1314. The method of any one of claims 1276-1290, wherein alkyl is butyl.
 1315. The method of any one of claims 1276-1290, wherein alkyl is pentyl.
 1316. The method of any one of claims 1276-1290, wherein alkyl is hexyl.
 1317. The method of any one of claims 1276-1290, wherein alkyl is heptyl.
 1318. The method of any one of claims 1276-1290, wherein alkyl is 2-phenylethyl.
 1319. The method of any one of claims 1276-1290, wherein alkyl is 2-methyloct-2-yl.
 1320. The method of any one of claims 16-1319, wherein the molecule has the chemical formula C_((MC))H_((MH))X_((MX))N_((MN))O_((MO))S_((MS)); the anion has the chemical formula C_((AC))H_((AH))X_((AX))N_((AN))O_((AO))S_((AS)) ¹⁻; MC is an integer from 6 to 32; MH is an integer from 6 to 50; MH is both at least half MC and no more than 1.75 times greater than MC; X is a halogen selected from F, Cl, Br, and I; MX is either 0, 1, or 2; MN is either 0, 1, or 2; MO is an integer from 1 to 12; MC is at least 2 times greater than MO; MS is either 0 or 1; AC equals MC; AH equals MH minus 1; AX equals MX; AN equals MN; AO equals MO; and AS equals MS.
 1321. The method of any one of claims 16-1320, wherein the molecule has the chemical formula C_((MC))H_((MH))N_((MN))O_((MO)); and the anion has the chemical formula C_((AC))H_((AH))N_((AN))O_((AO)) ¹⁻.
 1322. The method of any one of claims 16-1320, wherein the molecule has the chemical formula C_((MC))H_((MH))O_((MO))S_((MS)); and the anion has the chemical formula C_((AC))H_((AH))O_((AO))S(AS)¹⁻.
 1323. The method of any one of claims 16-1320, wherein the molecule has the chemical formula C_((MC))H_((MH))X_((MX))O_((MO)); and the anion has the chemical formula C_((AC))H_((AH))X_((AX))O_((AO)) ¹⁻.
 1324. The method of any one of claims 16-1320, wherein the molecule has the chemical formula C_((MC))H_((MH))O_((MO)); and the anion has the chemical formula C_((AC))H_((AH))O_((AO)) ¹⁻.
 1325. The method of any one of claims 1320-1324, wherein MC is
 16. 1326. The method of any one of claims 1320-1324, wherein MC is
 17. 1327. The method of any one of claims 1320-1324, wherein MC is
 18. 1328. The method of any one of claims 1320-1324, wherein MC is
 19. 1329. The method of any one of claims 1320-1324, wherein MC is
 20. 1330. The method of any one of claims 1320-1324, wherein MC is
 21. 1331. The method of any one of claims 1320-1324, wherein MC is
 22. 1332. The method of any one of claims 1320-1324, wherein MC is
 23. 1333. The method of any one of claims 1320-1324, wherein MC is
 24. 1334. The method of any one of claims 1320-1324, wherein MC is
 25. 1335. The method of any one of claims 1320-1324, wherein MC is
 26. 1336. The method of any one of claims 1320-1324, wherein MC is
 27. 1337. The method of any one of claims 1320-1324, wherein MC is
 28. 1338. The method of any one of claims 1320-1324, wherein MC is
 29. 1339. The method of any one of claims 1320-1324, wherein MC is
 30. 1340. The method of any one of claims 1320-1324, wherein MC is
 31. 1341. The method of any one of claims 1320-1324, wherein MC is
 32. 1342. The method of any one of claims 1320-1341, wherein MH is
 16. 1343. The method of any one of claims 1320-1341, wherein MH is
 17. 1344. The method of any one of claims 1320-1341, wherein MH is
 18. 1345. The method of any one of claims 1320-1341, wherein MH is
 19. 1346. The method of any one of claims 1320-1341, wherein MH is
 20. 1347. The method of any one of claims 1320-1341, wherein MH is
 21. 1348. The method of any one of claims 1320-1341, wherein MH is
 22. 1349. The method of any one of claims 1320-1341, wherein MH is
 23. 1350. The method of any one of claims 1320-1341, wherein MH is
 24. 1351. The method of any one of claims 1320-1341, wherein MH is
 25. 1352. The method of any one of claims 1320-1341, wherein MH is
 26. 1353. The method of any one of claims 1320-1341, wherein MH is
 27. 1354. The method of any one of claims 1320-1341, wherein MH is
 28. 1355. The method of any one of claims 1320-1341, wherein MH is
 29. 1356. The method of any one of claims 1320-1341, wherein MH is
 30. 1357. The method of any one of claims 1320-1341, wherein MH is
 31. 1358. The method of any one of claims 1320-1341, wherein MH is
 32. 1359. The method of any one of claims 1320-1341, wherein MH is
 33. 1360. The method of any one of claims 1320-1341, wherein MH is
 34. 1361. The method of any one of claims 1320-1341, wherein MH is
 35. 1362. The method of any one of claims 1320-1341, wherein MH is
 36. 1363. The method of any one of claims 1320-1341, wherein MH is
 37. 1364. The method of any one of claims 1320-1341, wherein MH is
 38. 1365. The method of any one of claims 1320-1341, wherein MH is
 39. 1366. The method of any one of claims 1320-1341, wherein MH is
 40. 1367. The method of any one of claims 1320-1341, wherein MH is
 41. 1368. The method of any one of claims 1320-1341, wherein MH is
 42. 1369. The method of any one of claims 1320-1341, wherein MH is
 43. 1370. The method of any one of claims 1320-1341, wherein MH is
 44. 1371. The method of any one of claims 1320-1341, wherein MH is
 45. 1372. The method of any one of claims 1320-1341, wherein MH is
 46. 1373. The method of any one of claims 1320-1341, wherein MH is
 47. 1374. The method of any one of claims 1320-1341, wherein MH is
 48. 1375. The method of any one of claims 1320-1341, wherein MH is
 49. 1376. The method of any one of claims 1320-1341, wherein MH is
 50. 1377. The method of any one of claims 1320-1341, wherein MH is
 51. 1378. The method of any one of claims 1320-1341, wherein MH is
 52. 1379. The method of any one of claims 1320-1341, wherein MH is
 53. 1380. The method of any one of claims 1320-1341, wherein MH is
 54. 1381. The method of any one of claims 1320-1341, wherein MH is
 55. 1382. The method of any one of claims 1320-1341, wherein MH is
 56. 1383. The method of any one of claims 1320-1341, wherein MH is
 57. 1384. The method of any one of claims 1320-1341, wherein MH is
 58. 1385. The method of any one of claims 1320-1341, wherein MH is
 59. 1386. The method of any one of claims 1320-1341, wherein MH is
 60. 1387. The method of any one of claims 1320-1341, wherein MH is
 61. 1388. The method of any one of claims 1320-1341, wherein MH is
 62. 1389. The method of any one of claims 1320-1388, wherein X is F.
 1390. The method of any one of claims 1320-1388, wherein X is Cl.
 1391. The method of any one of claims 1320-1388, wherein X is Br.
 1392. The method of any one of claims 1320-1388, wherein X is I.
 1393. The method of any one of claims 1320-1392, wherein MX is
 0. 1394. The method of any one of claims 1320-1392, wherein MX is
 1. 1395. The method of any one of claims 1320-1392, wherein MX is
 2. 1396. The method of any one of claims 1320-1395, wherein MN is
 0. 1397. The method of any one of claims 1320-1395, wherein MN is
 1. 1398. The method of any one of claims 1320-1395, wherein MN is
 2. 1399. The method of any one of claims 1320-1398, wherein MO is
 1. 1400. The method of any one of claims 1320-1398, wherein MO is
 2. 1401. The method of any one of claims 1320-1398, wherein MO is
 3. 1402. The method of any one of claims 1320-1398, wherein MO is
 4. 1403. The method of any one of claims 1320-1398, wherein MO is
 5. 1404. The method of any one of claims 1320-1398, wherein MO is
 6. 1405. The method of any one of claims 1320-1398, wherein MO is
 7. 1406. The method of any one of claims 1320-1398, wherein MO is
 8. 1407. The method of any one of claims 1320-1398, wherein MO is
 9. 1408. The method of any one of claims 1320-1398, wherein MO is
 10. 1409. The method of any one of claims 1320-1398, wherein MO is
 11. 1410. The method of any one of claims 1320-1398, wherein MO is
 12. 1411. The method of any one of claims 1320-1410, wherein MS is
 0. 1412. The method of any one of claims 1320-1410, wherein MS is
 1. 1413. The method of any one of claims 16-1412, wherein the molecule is CBD, THC, Δ8-THC, CBG, CBDV, THCV, Δ8-THCV, CBGV, CBC, CBN, tetrahydrocannabiphorol, perrottetinene, nabilone, parahexyl, HUM-217, or HU-331.
 1414. The method of any one of claims 16-1413, wherein the molecule is CBD.
 1415. The method of any one of claims 16-1413, wherein the molecule is THC.
 1416. The method of any one of claims 16-1413, wherein the molecule is Δ8-THC.
 1417. The method of any one of claims 16-1413, wherein the molecule is CBG.
 1418. The method of any one of claims 16-1413, wherein the molecule is CBDV.
 1419. The method of any one of claims 16-1413, wherein the molecule is THCV.
 1420. The method of any one of claims 16-1413, wherein the molecule is Δ8-THCV.
 1421. The method of any one of claims 16-1413, wherein the molecule is CBGV.
 1422. The method of any one of claims 16-1413, wherein the molecule is CBC.
 1423. The method of any one of claims 16-1413, wherein the molecule is CBN.
 1424. The method of any one of claims 16-1413, wherein the molecule is tetrahydrocannabiphorol.
 1425. The method of any one of claims 16-1413, wherein the molecule is perrottetinene.
 1426. The method of any one of claims 16-1413, wherein the molecule is nabilone.
 1427. The method of any one of claims 16-1413, wherein the molecule is parahexyl.
 1428. The method of any one of claims 16-1413, wherein the molecule is HUM-217.
 1429. The method of any one of claims 16-1413, wherein the molecule is HU-331.
 1430. The method of any one of claims 3-1429, wherein at least one carbohydrate of the carbohydrates has the chemical formula CxHyOz; x is an integer greater than 3; y is an integer greater than 1.3x and no greater than 2x+2; and z is an integer of at least 0.7x and no greater than x.
 1431. The method of any one of claims 3-1430, wherein each carbohydrate of the carbohydrates has the chemical formula CxHyOz; x is an integer greater than 3; y is an integer greater than 1.3x and no greater than 2x+2; and z is an integer of at least 0.7x and no greater than x.
 1432. The method of any one of claims 3-1431, wherein at least one carbohydrate of the carbohydrates has the chemical formula CxHyOz; x is an integer greater than 3 and no greater than 12; y is an integer greater than 1.8x and no greater than 2x+2; and z is an integer of at least 0.8x and no greater than x.
 1433. The method of any one of claims 3-1432, wherein each carbohydrate of the carbohydrates has the chemical formula CxHyOz; x is an integer greater than 3 and no greater than 12; y is an integer greater than 1.8x and no greater than 2x+2; and z is an integer of at least 0.8x and no greater than x.
 1434. The method of any one of claims 3-1433, wherein the carbohydrates comprise one or more polysaccharides, sulfated polysaccharides, oligosaccharides, disaccharides, monosaccharides, and sugar alcohols.
 1435. The method of any one of claims 3-1434, wherein the carbohydrates consist of one or more polysaccharides, sulfated polysaccharides, oligosaccharides, disaccharides, monosaccharides, and sugar alcohols.
 1436. The method of any one of claims 3-1435, wherein the carbohydrates comprise one or more of alginic acid, alginate, propylene glycol alginate, inulin, arabinogalactan, lignosulfonate, carrageenan, furcelleran, pullulan, glucomannan, gellan gum, gum arabic, gellan gum, gum ghatti, guar gum, gum karaya, tara gum, tragacanth, xanthan gum, carboxymethylcellulose, hydroxyethyl cellulose, ethylhydroxyethylcellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, modified starch, dextrin, polydextrose, pectin, beta-glucan, lactobionic acid, lactobionate, isomalt, erythritol, threitol, arabitol, xylitol, ribitol, mannitol, sorbitol, galactitol, fucitol, iditol, inositol, volemitol, sucrose, lactose, maltose, trehalose, maltitol, glucose, fructose, galactose, arabinose, ribose, xylose, allulose, sorbose, tagatose, fucose, mannose, and hydrogenated starch hydrolysate.
 1437. The method of any one of claims 3-1436, wherein the carbohydrates consist of one or more of alginic acid, alginate, propylene glycol alginate, inulin, arabinogalactan, lignosulfonate, carrageenan, furcelleran, pullulan, glucomannan, gellan gum, gum arabic, gellan gum, gum ghatti, guar gum, gum karaya, tara gum, tragacanth, xanthan gum, carboxymethylcellulose, hydroxyethyl cellulose, ethylhydroxyethylcellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, modified starch, dextrin, polydextrose, pectin, beta-glucan, lactobionic acid, lactobionate, isomalt, erythritol, threitol, arabitol, xylitol, ribitol, mannitol, sorbitol, galactitol, fucitol, iditol, inositol, volemitol, sucrose, lactose, maltose, trehalose, maltitol, glucose, fructose, galactose, arabinose, ribose, xylose, allulose, sorbose, tagatose, fucose, mannose, and hydrogenated starch hydrolysate.
 1438. The method of any one of claims 3-1437, wherein the carbohydrates comprise alginic acid.
 1439. The method of any one of claims 3-1438, wherein the carbohydrates comprise alginate.
 1440. The method of any one of claims 3-1439, wherein the carbohydrates comprise propylene glycol alginate.
 1441. The method of any one of claims 3-1440, wherein the carbohydrates comprise inulin.
 1442. The method of any one of claims 3-1441, wherein the carbohydrates comprise arabinogalactan.
 1443. The method of any one of claims 3-1442, wherein the carbohydrates comprise lignosulfonate.
 1444. The method of any one of claims 3-1443, wherein the carbohydrates comprise carrageenan.
 1445. The method of any one of claims 3-1444, wherein the carbohydrates comprise furcelleran.
 1446. The method of any one of claims 3-1445, wherein the carbohydrates comprise pullulan.
 1447. The method of any one of claims 3-1446, wherein the carbohydrates comprise glucomannan.
 1448. The method of any one of claims 3-1447, wherein the carbohydrates comprise gellan gum.
 1449. The method of any one of claims 3-1448, wherein the carbohydrates comprise gum arabic.
 1450. The method of any one of claims 3-1449, wherein the carbohydrates comprise gellan gum.
 1451. The method of any one of claims 3-1450, wherein the carbohydrates comprise gum ghatti.
 1452. The method of any one of claims 3-1451, wherein the carbohydrates comprise guar gum.
 1453. The method of any one of claims 3-1452, wherein the carbohydrates comprise gum karaya.
 1454. The method of any one of claims 3-1453, wherein the carbohydrates comprise tara gum.
 1455. The method of any one of claims 3-1454, wherein the carbohydrates comprise tragacanth.
 1456. The method of any one of claims 3-1455, wherein the carbohydrates comprise xanthan gum.
 1457. The method of any one of claims 3-1456, wherein the carbohydrates comprise carboxymethylcellulose.
 1458. The method of any one of claims 3-1457, wherein the carbohydrates comprise hydroxyethyl cellulose.
 1459. The method of any one of claims 3-1458, wherein the carbohydrates comprise ethylhydroxyethylcellulose.
 1460. The method of any one of claims 3-1459, wherein the carbohydrates comprise hydroxypropyl cellulose.
 1461. The method of any one of claims 3-1460, wherein the carbohydrates comprise hydroxypropyl methylcellulose.
 1462. The method of any one of claims 3-1461, wherein the carbohydrates comprise modified starch.
 1463. The method of any one of claims 3-1462, wherein the carbohydrates comprise dextrin.
 1464. The method of any one of claims 3-1463, wherein the carbohydrates comprise polydextrose.
 1465. The method of any one of claims 3-1464, wherein the carbohydrates comprise pectin.
 1466. The method of any one of claims 3-1465, wherein the carbohydrates comprise beta-glucan.
 1467. The method of any one of claims 3-1466, wherein the carbohydrates comprise lactobionic acid.
 1468. The method of any one of claims 3-1467, wherein the carbohydrates comprise lactobionate.
 1469. The method of any one of claims 3-1468, wherein the carbohydrates comprise isomalt.
 1470. The method of any one of claims 3-1469, wherein the carbohydrates comprise butane-1,2,3,4-tetrol.
 1471. The method of claim 1470, wherein the liquid phase comprises butane-1,2,3,4-tetrol and one or both of 1,3,4-trihydroxybutane-2-oxide and 2,3,4-trihydroxybutane-1-oxide.
 1472. The method of claim 1470 or 1471, wherein the liquid phase comprises butane-1,2,3,4-tetrol and one or both of 1,3,4-trihydroxybutane-2-oxide and 2,3,4-trihydroxybutane-1-oxide at a ratio of at least 100:1 and no greater than 10,000,000:1 (butane-1,2,3,4-tetrol: 1,3,4-trihydroxybutane-2-oxide and 2,3,4-trihydroxybutane-1-oxide).
 1473. The method of any one of claims 1470-1472, wherein the liquid phase comprises butane-1,2,3,4-tetrol and one or both of 1,3,4-trihydroxybutane-2-oxide and 2,3,4-trihydroxybutane-1-oxide at a ratio of at least 100:1 and no greater than 1,000,000:1 (butane-1,2,3,4-tetrol: 1,3,4-trihydroxybutane-2-oxide and 2,3,4-trihydroxybutane-1-oxide).
 1474. The method of any one of claims 1470-1473, wherein the liquid phase comprises butane-1,2,3,4-tetrol and one or both of 1,3,4-trihydroxybutane-2-oxide and 2,3,4-trihydroxybutane-1-oxide at a ratio of at least 100:1 and no greater than 100,000:1 (butane-1,2,3,4-tetrol: 1,3,4-trihydroxybutane-2-oxide and 2,3,4-trihydroxybutane-1-oxide).
 1475. The method of any one of claims 1470-1474, wherein the butane-1,2,3,4-tetrol comprises one or both of erythritol and threitol.
 1476. The method of any one of claims 1470-1475, wherein the butane-1,2,3,4-tetrol is erythritol.
 1477. The method of any one of claims 1470-1476, wherein the butane-1,2,3,4-tetrol is threitol.
 1478. The method of any one of claims 3-1477, wherein the carbohydrates comprise pentane-1,2,3,4,5-pentol.
 1479. The method of claim 1478, wherein the liquid phase comprises pentane-1,2,3,4,5-pentol and one, two, or each of 1,2,4,5-tetrahydroxypentane-3-oxide, 1,3,4,5-tetrahydroxypentane-2-oxide, and 2,3,4,5-tetrahydroxypentane-1-oxide.
 1480. The method of claim 1478 or 1479, wherein the liquid phase comprises pentane-1,2,3,4,5-pentol and one, two, or each of 1,2,4,5-tetrahydroxypentane-3-oxide, 1,3,4,5-tetrahydroxypentane-2-oxide, and 2,3,4,5-tetrahydroxypentane-1-oxide at a ratio of at least 100:1 and no greater than 10,000,000:1 (pentane-1,2,3,4,5-pentol:1,2,4,5-tetrahydroxypentane-3-oxide, 1,3,4,5-tetrahydroxypentane-2-oxide, and 2,3,4,5-tetrahydroxypentane-1-oxide).
 1481. The method of any one of claims 1478-1480, wherein the liquid phase comprises pentane-1,2,3,4,5-pentol and one, two, or each of 1,2,4,5-tetrahydroxypentane-3-oxide, 1,3,4,5-tetrahydroxypentane-2-oxide, and 2,3,4,5-tetrahydroxypentane-1-oxide at a ratio of at least 100:1 and no greater than 1,000,000:1 (pentane-1,2,3,4,5-pentol:1,2,4,5-tetrahydroxypentane-3-oxide, 1,3,4,5-tetrahydroxypentane-2-oxide, and 2,3,4,5-tetrahydroxypentane-1-oxide).
 1482. The method of any one of claims 1478-1481, wherein the liquid phase comprises pentane-1,2,3,4,5-pentol and one, two, or each of 1,2,4,5-tetrahydroxypentane-3-oxide, 1,3,4,5-tetrahydroxypentane-2-oxide, and 2,3,4,5-tetrahydroxypentane-1-oxide at a ratio of at least 100:1 and no greater than 100,000:1 (pentane-1,2,3,4,5-pentol:1,2,4,5-tetrahydroxypentane-3-oxide, 1,3,4,5-tetrahydroxypentane-2-oxide, and 2,3,4,5-tetrahydroxypentane-1-oxide).
 1483. The method of any one of claims 1478-1482, wherein the pentane-1,2,3,4,5-pentol comprises one, two, or each of arabitol, xylitol, and ribitol.
 1484. The method of any one of claims 1478-1483, wherein the pentane-1,2,3,4,5-pentol is arabitol.
 1485. The method of any one of claims 1478-1484, wherein the pentane-1,2,3,4,5-pentol is xylitol.
 1486. The method of any one of claims 1478-1485, wherein the pentane-1,2,3,4,5-pentol is ribitol.
 1487. The method of any one of claims 3-1486, wherein the carbohydrates comprise hexane-1,2,3,4,5,6-hexol.
 1488. The method of claim 1487, wherein the liquid phase comprises hexane-1,2,3,4,5,6-hexol and one, two, or each of 1,2,4,5,6-pentahydroxyhexane-3-oxide, 1,3,4,5,6-pentahydroxyhexane-2-oxide, and 2,3,4,5,6-pentahydroxyhexane-1-oxide.
 1489. The method of claim 1487 or 1488, wherein the liquid phase comprises hexane-1,2,3,4,5,6-hexol and one, two, or each of 1,2,4,5,6-pentahydroxyhexane-3-oxide, 1,3,4,5,6-pentahydroxyhexane-2-oxide, and 2,3,4,5,6-pentahydroxyhexane-1-oxide at a ratio of at least 100:1 and no greater than 10,000,000:1 (hexane-1,2,3,4,5,6-hexol:1,2,4,5,6-pentahydroxyhexane-3-oxide, 1,3,4,5,6-pentahydroxyhexane-2-oxide, and 2,3,4,5,6-pentahydroxyhexane-1-oxide).
 1490. The method of any one of claims 1487-1489, wherein the liquid phase comprises hexane-1,2,3,4,5,6-hexol and one, two, or each of 1,2,4,5,6-pentahydroxyhexane-3-oxide, 1,3,4,5,6-pentahydroxyhexane-2-oxide, and 2,3,4,5,6-pentahydroxyhexane-1-oxide at a ratio of at least 100:1 and no greater than 1,000,000:1 (hexane-1,2,3,4,5,6-hexol:1,2,4,5,6-pentahydroxyhexane-3-oxide, 1,3,4,5,6-pentahydroxyhexane-2-oxide, and 2,3,4,5,6-pentahydroxyhexane-1-oxide).
 1491. The method of any one of claims 1487-1490, wherein the liquid phase comprises hexane-1,2,3,4,5,6-hexol and one, two, or each of 1,2,4,5,6-pentahydroxyhexane-3-oxide, 1,3,4,5,6-pentahydroxyhexane-2-oxide, and 2,3,4,5,6-pentahydroxyhexane-1-oxide at a ratio of at least 100:1 and no greater than 100,000:1 (hexane-1,2,3,4,5,6-hexol:1,2,4,5,6-pentahydroxyhexane-3-oxide, 1,3,4,5,6-pentahydroxyhexane-2-oxide, and 2,3,4,5,6-pentahydroxyhexane-1-oxide).
 1492. The method of any one of claims 1487-1491, wherein the hexane-1,2,3,4,5,6-hexol comprises one, two, three, four, or each of mannitol, sorbitol, galactitol, fucitol, and iditol.
 1493. The method of any one of claims 1487-1492, wherein the hexane-1,2,3,4,5,6-hexol is mannitol.
 1494. The method of any one of claims 1487-1493, wherein the hexane-1,2,3,4,5,6-hexol is sorbitol.
 1495. The method of any one of claims 1487-1494, wherein the hexane-1,2,3,4,5,6-hexol is galactitol.
 1496. The method of any one of claims 1487-1495, wherein the hexane-1,2,3,4,5,6-hexol is fucitol.
 1497. The method of any one of claims 1487-1496, wherein the hexane-1,2,3,4,5,6-hexol is iditol.
 1498. The method of any one of claims 3-1497, wherein the carbohydrates comprise cyclohexane-1,2,3,4,5,6-hexol.
 1499. The method of claim 1498, wherein the liquid phase comprises cyclohexane-1,2,3,4,5,6-hexol and 2,3,4,5,6-pentahydroxycyclohexane-1-oxide.
 1500. The method of claim 1498 or 1499, wherein the liquid phase comprises cyclohexane-1,2,3,4,5,6-hexol and 2,3,4,5,6-pentahydroxycyclohexane-1-oxide at a ratio of at least 100:1 and no greater than 10,000,000:1.
 1501. The method of any one of claims 1498-1500, wherein the liquid phase comprises cyclohexane-1,2,3,4,5,6-hexol and 2,3,4,5,6-pentahydroxycyclohexane-1-oxide at a ratio of at least 100:1 and no greater than 1,000,000:1.
 1502. The method of any one of claims 1498-1501, wherein the liquid phase comprises cyclohexane-1,2,3,4,5,6-hexol and 2,3,4,5,6-pentahydroxycyclohexane-1-oxide at a ratio of at least 100:1 and no greater than 100,000:1.
 1503. The method of any one of claims 1498-1502, wherein the cyclohexane-1,2,3,4,5,6-hexol comprises inositol.
 1504. The method of any one of claims 1498-1503, wherein the cyclohexane-1,2,3,4,5,6-hexol is inositol.
 1505. The method of any one of claims 3-1504, wherein the carbohydrates comprise heptane-1,2,3,4,5,6,7-heptol.
 1506. The method of claim 1505, wherein the liquid phase comprises heptane-1,2,3,4,5,6,7-heptol and one, two, three, or each of 1,2,3,5,6,7-hexahydroxyheptane-4-oxide, 1,2,4,5,6,7-hexahydroxyheptane-3-oxide, 1,3,4,5,6,7-hexahydroxyheptane-2-oxide, and 2,3,4,5,6,7-hexahydroxyheptane-1-oxide.
 1507. The method of claim 1505 or 1506, wherein the liquid phase comprises heptane-1,2,3,4,5,6,7-heptol and one, two, three, or each of 1,2,3,5,6,7-hexahydroxyheptane-4-oxide, 1,2,4,5,6,7-hexahydroxyheptane-3-oxide, 1,3,4,5,6,7-hexahydroxyheptane-2-oxide, and 2,3,4,5,6,7-hexahydroxyheptane-1-oxide at a ratio of at least 100:1 and no greater than 10,000,000:1 (heptane-1,2,3,4,5,6,7-heptol:1,2,3,5,6,7-hexahydroxyheptane-4-oxide, 1,2,4,5,6,7-hexahydroxyheptane-3-oxide, 1,3,4,5,6,7-hexahydroxyheptane-2-oxide, and 2,3,4,5,6,7-hexahydroxyheptane-1-oxide).
 1508. The method of any one of claims 1505-1507, wherein the liquid phase comprises heptane-1,2,3,4,5,6,7-heptol and one, two, three, or each of 1,2,3,5,6,7-hexahydroxyheptane-4-oxide, 1,2,4,5,6,7-hexahydroxyheptane-3-oxide, 1,3,4,5,6,7-hexahydroxyheptane-2-oxide, and 2,3,4,5,6,7-hexahydroxyheptane-1-oxide at a ratio of at least 100:1 and no greater than 1,000,000:1 (heptane-1,2,3,4,5,6,7-heptol:1,2,3,5,6,7-hexahydroxyheptane-4-oxide, 1,2,4,5,6,7-hexahydroxyheptane-3-oxide, 1,3,4,5,6,7-hexahydroxyheptane-2-oxide, and 2,3,4,5,6,7-hexahydroxyheptane-1-oxide).
 1509. The method of any one of claims 1505-1508, wherein the liquid phase comprises heptane-1,2,3,4,5,6,7-heptol and one, two, three, or each of 1,2,3,5,6,7-hexahydroxyheptane-4-oxide, 1,2,4,5,6,7-hexahydroxyheptane-3-oxide, 1,3,4,5,6,7-hexahydroxyheptane-2-oxide, and 2,3,4,5,6,7-hexahydroxyheptane-1-oxide at a ratio of at least 100:1 and no greater than 100,000:1 (heptane-1,2,3,4,5,6,7-heptol:1,2,3,5,6,7-hexahydroxyheptane-4-oxide, 1,2,4,5,6,7-hexahydroxyheptane-3-oxide, 1,3,4,5,6,7-hexahydroxyheptane-2-oxide, and 2,3,4,5,6,7-hexahydroxyheptane-1-oxide).
 1510. The method of any one of claims 1505-1509, wherein the heptane-1,2,3,4,5,6,7-heptol comprises volemitol.
 1511. The method of any one of claims 1505-1510, wherein the heptane-1,2,3,4,5,6,7-heptol is volemitol.
 1512. The method of any one of claims 3-1511, wherein the carbohydrates comprise sucrose.
 1513. The method of any one of claims 3-1512, wherein the carbohydrates comprise lactose.
 1514. The method of any one of claims 3-1513, wherein the carbohydrates comprise maltose.
 1515. The method of any one of claims 3-1514, wherein the carbohydrates comprise trehalose.
 1516. The method of any one of claims 3-1515, wherein the carbohydrates comprise maltitol.
 1517. The method of any one of claims 3-1516, wherein the carbohydrates comprise glucose.
 1518. The method of any one of claims 3-1517, wherein the carbohydrates comprise fructose.
 1519. The method of any one of claims 3-1518, wherein the carbohydrates comprise galactose.
 1520. The method of any one of claims 3-1519, wherein the carbohydrates comprise arabinose.
 1521. The method of any one of claims 3-1520, wherein the carbohydrates comprise ribose.
 1522. The method of any one of claims 3-1521, wherein the carbohydrates comprise xylose.
 1523. The method of any one of claims 3-1522, wherein the carbohydrates comprise allulose.
 1524. The method of any one of claims 3-1523, wherein the carbohydrates comprise sorbose.
 1525. The method of any one of claims 3-1524, wherein the carbohydrates comprise tagatose.
 1526. The method of any one of claims 3-1525, wherein the carbohydrates comprise fucose.
 1527. The method of any one of claims 3-1526, wherein the carbohydrates comprise mannose.
 1528. The method of any one of claims 3-1527, wherein the carbohydrates comprise hydrogenated starch hydrolysate.
 1529. The method of any one of claims 3-1437, wherein the carbohydrates consist of alginic acid.
 1530. The method of any one of claims 3-1437, wherein the carbohydrates consist of alginate.
 1531. The method of any one of claims 3-1437, wherein the carbohydrates consist of propylene glycol alginate.
 1532. The method of any one of claims 3-1437, wherein the carbohydrates consist of inulin.
 1533. The method of any one of claims 3-1437, wherein the carbohydrates consist of arabinogalactan.
 1534. The method of any one of claims 3-1437, wherein the carbohydrates consist of lignosulfonate.
 1535. The method of any one of claims 3-1437, wherein the carbohydrates consist of carrageenan.
 1536. The method of any one of claims 3-1437, wherein the carbohydrates consist of furcelleran.
 1537. The method of any one of claims 3-1437, wherein the carbohydrates consist of pullulan.
 1538. The method of any one of claims 3-1437, wherein the carbohydrates consist of glucomannan.
 1539. The method of any one of claims 3-1437, wherein the carbohydrates consist of gellan gum.
 1540. The method of any one of claims 3-1437, wherein the carbohydrates consist of gum arabic.
 1541. The method of any one of claims 3-1437, wherein the carbohydrates consist of gellan gum.
 1542. The method of any one of claims 3-1437, wherein the carbohydrates consist of gum ghatti.
 1543. The method of any one of claims 3-1437, wherein the carbohydrates consist of guar gum.
 1544. The method of any one of claims 3-1437, wherein the carbohydrates consist of gum karaya.
 1545. The method of any one of claims 3-1437, wherein the carbohydrates consist of tara gum.
 1546. The method of any one of claims 3-1437, wherein the carbohydrates consist of tragacanth.
 1547. The method of any one of claims 3-1437, wherein the carbohydrates consist of xanthan gum.
 1548. The method of any one of claims 3-1437, wherein the carbohydrates consist of carboxymethylcellulose.
 1549. The method of any one of claims 3-1437, wherein the carbohydrates consist of hydroxyethyl cellulose.
 1550. The method of any one of claims 3-1437, wherein the carbohydrates consist of ethylhydroxyethylcellulose.
 1551. The method of any one of claims 3-1437, wherein the carbohydrates consist of hydroxypropyl cellulose.
 1552. The method of any one of claims 3-1437, wherein the carbohydrates consist of hydroxypropyl methylcellulose.
 1553. The method of any one of claims 3-1437, wherein the carbohydrates consist of modified starch.
 1554. The method of any one of claims 3-1437, wherein the carbohydrates consist of dextrin.
 1555. The method of any one of claims 3-1437, wherein the carbohydrates consist of polydextrose.
 1556. The method of any one of claims 3-1437, wherein the carbohydrates consist of pectin.
 1557. The method of any one of claims 3-1437, wherein the carbohydrates consist of beta-glucan.
 1558. The method of any one of claims 3-1437, wherein the carbohydrates consist of lactobionic acid.
 1559. The method of any one of claims 3-1437, wherein the carbohydrates consist of lactobionate.
 1560. The method of any one of claims 3-1437, wherein the carbohydrates consist of isomalt.
 1561. The method of any one of claims 3-1437 and 1470-1477, wherein the carbohydrates consist of butane-1,2,3,4-tetrol.
 1562. The method of any one of claims 3-1437 and 1478-1486, wherein the carbohydrates consist of pentane-1,2,3,4,5-pentol.
 1563. The method of any one of claims 3-1437 and 1487-1497, wherein the carbohydrates consist of hexane-1,2,3,4,5,6-hexol.
 1564. The method of any one of claims 3-1437 and 1498-1504, wherein the carbohydrates consist of cyclohexane-1,2,3,4,5,6-hexol.
 1565. The method of any one of claims 3-1437 and 1505-1511, wherein the carbohydrates consist of heptane-1,2,3,4,5,6,7-heptol.
 1566. The method of any one of claims 3-1437, wherein the carbohydrates consist of sucrose.
 1567. The method of any one of claims 3-1437, wherein the carbohydrates consist of lactose.
 1568. The method of any one of claims 3-1437, wherein the carbohydrates consist of maltose.
 1569. The method of any one of claims 3-1437, wherein the carbohydrates consist of trehalose.
 1570. The method of any one of claims 3-1437, wherein the carbohydrates consist of maltitol.
 1571. The method of any one of claims 3-1437, wherein the carbohydrates consist of glucose.
 1572. The method of any one of claims 3-1437, wherein the carbohydrates consist of fructose.
 1573. The method of any one of claims 3-1437, wherein the carbohydrates consist of galactose.
 1574. The method of any one of claims 3-1437, wherein the carbohydrates consist of arabinose.
 1575. The method of any one of claims 3-1437, wherein the carbohydrates consist of ribose.
 1576. The method of any one of claims 3-1437, wherein the carbohydrates consist of xylose.
 1577. The method of any one of claims 3-1437, wherein the carbohydrates consist of allulose.
 1578. The method of any one of claims 3-1437, wherein the carbohydrates consist of sorbose.
 1579. The method of any one of claims 3-1437, wherein the carbohydrates consist of tagatose.
 1580. The method of any one of claims 3-1437, wherein the carbohydrates consist of fucose.
 1581. The method of any one of claims 3-1437, wherein the carbohydrates consist of mannose.
 1582. The method of any one of claims 3-1437, wherein the carbohydrates consist of hydrogenated starch hydrolysate.
 1583. The method of any one of claims 3-1582, wherein at least one carbohydrate of the carbohydrates is present both in the solid phase as a solid and in the liquid phase as a solute.
 1584. The method of any one of claims 3-1583, wherein at least one carbohydrate of the carbohydrates is present both in the solid phase as a solid and in the liquid phase as a solute; the carbohydrate that is present both in the solid phase and in the liquid phase has a solubility in the liquid phase and a concentration in the liquid phase; and the concentration of the carbohydrate in the liquid phase is at least 10 and no greater than 110 percent of the solubility of the carbohydrate in the liquid phase.
 1585. The method of any one of claims 3-1584, wherein at least one carbohydrate of the carbohydrates is present both in the solid phase as a solid and in the liquid phase as a solute; the carbohydrate that is present both in the solid phase and in the liquid phase has a solubility in the liquid phase and a concentration in the liquid phase; and the concentration of the carbohydrate in the liquid phase is at least 80 and no greater than 105 percent of the solubility of the carbohydrate in the liquid phase.
 1586. The method of any one of claims 3-1585, wherein at least one carbohydrate of the carbohydrates is present both in the solid phase as a solid and in the liquid phase as a solute; the carbohydrate that is present both in the solid phase and in the liquid phase has a solubility in the liquid phase and a concentration in the liquid phase; and the concentration of the carbohydrate in the liquid phase is at least 90 and no greater than 100 percent of the solubility of the carbohydrate in the liquid phase.
 1587. The method of any one of claims 3-1586, wherein the carbohydrates are present both in the solid phase as solids and in the liquid phase as solutes.
 1588. The method of any one of claims 3-1587, wherein the carbohydrates are present both in the solid phase as solids and in the liquid phase as solutes; each carbohydrate of the carbohydrates has a solubility in the liquid phase and a concentration in the liquid phase; and the concentration of each carbohydrate in the liquid phase is at least 10 and no greater than 110 percent of the solubility of the carbohydrate in the liquid phase.
 1589. The method of any one of claims 3-1588, wherein the carbohydrates are present both in the solid phase as solids and in the liquid phase as solutes; each carbohydrate of the carbohydrates has a solubility in the liquid phase and a concentration in the liquid phase; and the concentration of each carbohydrate in the liquid phase is at least 80 and no greater than 105 percent of the solubility of the carbohydrate in the liquid phase.
 1590. The method of any one of claims 3-1589, wherein the carbohydrates are present both in the solid phase as solids and in the liquid phase as solutes; each carbohydrate of the carbohydrates has a solubility in the liquid phase and a concentration in the liquid phase; and the concentration of each carbohydrate in the liquid phase is at least 90 and no greater than 100 percent of the solubility of the carbohydrate in the liquid phase.
 1591. The method of any one of claims 3-1590, wherein the beverage formulation is effective to treat a health condition in a human.
 1592. The method of any one of claims 3-1591, wherein the beverage formulation is effective to prophylactically prevent a health condition in a human.
 1593. The method of claim 1591 or 1592, wherein the health condition is type 2 diabetes mellitus.
 1594. The method of claim 1591 or 1592, wherein the health condition is metabolic syndrome.
 1595. The method of claim 1591 or 1592, wherein the health condition is hypertension.
 1596. The method of claim 1591 or 1592, wherein the health condition is pre-hypertension.
 1597. The method of claim 1591 or 1592, wherein the health condition is a neurodegenerative disease or neuropathy.
 1598. The method of claim 1591 or 1592, wherein the health condition is mild cognitive impairment.
 1599. The method of claim 1591 or 1592, wherein the health condition is Alzheimer's Disease.
 1600. The method of claim 1591 or 1592, wherein the health condition is Parkinson's Disease.
 1601. The method of claim 1591 or 1592, wherein the health condition is amyotrophic lateral sclerosis (“ALS”).
 1602. The method of claim 1591 or 1592, wherein the health condition is Huntington's disease.
 1603. The method of claim 1591 or 1592, wherein the health condition is an autoimmune disorder.
 1604. The method of claim 1591 or 1592, wherein the health condition is arthritis.
 1605. The method of claim 1591 or 1592, wherein the health condition is ankylosing spondylitis.
 1606. The method of claim 1591 or 1592, wherein the health condition is an inflammatory autoimmune-mediated arthritis.
 1607. The method of claim 1591 or 1592, wherein the health condition is rheumatoid arthritis.
 1608. The method of claim 1591 or 1592, wherein the health condition is psoriatic arthritis.
 1609. The method of claim 1591 or 1592, wherein the health condition is psoriasis.
 1610. The method of claim 1591 or 1592, wherein the health condition is plaque psoriasis.
 1611. The method of claim 1591 or 1592, wherein the health condition is lupus.
 1612. The method of claim 1591 or 1592, wherein the health condition is Sjogren's syndrome.
 1613. The method of claim 1591 or 1592, wherein the health condition is inflammatory bowel disease.
 1614. The method of claim 1591 or 1592, wherein the health condition is Crohn's disease.
 1615. The method of claim 1591 or 1592, wherein the health condition is ulcerative colitis.
 1616. The method of claim 1591 or 1592, wherein the health condition is a headache.
 1617. The method of claim 1591 or 1592, wherein the health condition is a migraine headache.
 1618. The method of claim 1591 or 1592, wherein the health condition is an episodic migraine.
 1619. The method of claim 1591 or 1592, wherein the health condition is pain.
 1620. The method of claim 1591 or 1592, wherein the health condition is nociceptive pain.
 1621. The method of claim 1591 or 1592, wherein the health condition is allodynia.
 1622. The method of claim 1591 or 1592, wherein the health condition is chronic pain.
 1623. The method of claim 1591 or 1592, wherein the health condition is intractable pain.
 1624. The method of claim 1591 or 1592, wherein the health condition is back pain.
 1625. The method of claim 1591 or 1592, wherein the health condition is lower back pain.
 1626. The method of claim 1591 or 1592, wherein the health condition is chronic back pain.
 1627. The method of claim 1591 or 1592, wherein the health condition is sciatica.
 1628. The method of claim 1591 or 1592, wherein the health condition is spinal stenosis.
 1629. The method of claim 1591 or 1592, wherein the health condition is chronic radiculopathy.
 1630. The method of claim 1591 or 1592, wherein the health condition is post laminectomy syndrome.
 1631. The method of claim 1591 or 1592, wherein the health condition is stomach pain.
 1632. The method of claim 1591 or 1592, wherein the health condition is visceral pain.
 1633. The method of claim 1591 or 1592, wherein the health condition is interstitial cystitis.
 1634. The method of claim 1591 or 1592, wherein the health condition is postherpetic neuralgia.
 1635. The method of claim 1591 or 1592, wherein the health condition is sickle cell anemia.
 1636. The method of claim 1591 or 1592, wherein the health condition is sickle cell disease.
 1637. The method of claim 1591 or 1592, wherein the health condition is cancer pain.
 1638. The method of claim 1591 or 1592, wherein the health condition is intractable cancer pain.
 1639. The method of claim 1591 or 1592, wherein the health condition is fibromyalgia.
 1640. The method of claim 1591 or 1592, wherein the health condition is neurogenic pain.
 1641. The method of claim 1591 or 1592, wherein the health condition is neuropathic pain.
 1642. The method of claim 1591 or 1592, wherein the health condition is peripheral neuropathy.
 1643. The method of claim 1591 or 1592, wherein the health condition is inflammatory demyelinating polyneuropathy.
 1644. The method of claim 1591 or 1592, wherein the health condition is peripheral pain.
 1645. The method of claim 1591 or 1592, wherein the health condition is reflex sympathetic dystrophy.
 1646. The method of claim 1591 or 1592, wherein the health condition is residual limb pain.
 1647. The method of claim 1591 or 1592, wherein the health condition is idiopathic pain.
 1648. The method of claim 1591 or 1592, wherein the health condition is psychogenic pain.
 1649. The method of claim 1591 or 1592, wherein the health condition is causalgia.
 1650. The method of claim 1591 or 1592, wherein the health condition is complex regional pain syndrome.
 1651. The method of claim 1591 or 1592, wherein the health condition is complex regional pain syndrome type I.
 1652. The method of claim 1591 or 1592, wherein the health condition is complex regional pain syndrome type II.
 1653. The method of claim 1591 or 1592, wherein the health condition is gout.
 1654. The method of claim 1591 or 1592, wherein the health condition is epidermolysis bullosa.
 1655. The method of claim 1591 or 1592, wherein the health condition is hemorrhoids.
 1656. The method of claim 1591 or 1592, wherein the health condition is constipation.
 1657. The method of claim 1591 or 1592, wherein the health condition is elevated intraocular pressure.
 1658. The method of claim 1591 or 1592, wherein the health condition is glaucoma.
 1659. The method of claim 1591 or 1592, wherein the health condition is liver disease.
 1660. The method of claim 1591 or 1592, wherein the health condition is non-alcoholic fatty liver disease (“NAFLD”).
 1661. The method of claim 1591 or 1592, wherein the health condition is non-alcoholic steatohepatitis (“NASH”).
 1662. The method of claim 1591 or 1592, wherein the health condition is liver cirrhosis.
 1663. The method of claim 1591 or 1592, wherein the health condition is decompensated cirrhosis.
 1664. The method of claim 1591 or 1592, wherein the health condition is hepatic encephalopathy.
 1665. The method of claim 1591 or 1592, wherein the health condition is hepatitis.
 1666. The method of claim 1591 or 1592, wherein the health condition is hepatitis C.
 1667. The method of claim 1591 or 1592, wherein the health condition is nausea.
 1668. The method of claim 1591 or 1592, wherein the health condition is cachexia.
 1669. The method of claim 1591 or 1592, wherein the health condition is anorexia.
 1670. The method of claim 1591 or 1592, wherein the health condition is bulimia.
 1671. The method of claim 1591 or 1592, wherein the health condition is vomiting.
 1672. The method of claim 1591 or 1592, wherein the health condition is motion sickness.
 1673. The method of claim 1591 or 1592, wherein the health condition is cancer chemotherapy-induced anorexia.
 1674. The method of claim 1591 or 1592, wherein the health condition is human deficiency virus (“HIV”) infection related nausea or cachexia.
 1675. The method of claim 1591 or 1592, wherein the health condition is acquired immune deficiency syndrome (“AIDS”) related nausea or cachexia.
 1676. The method of claim 1591 or 1592, wherein the health condition is anxiety.
 1677. The method of claim 1591 or 1592, wherein the health condition is generalized anxiety disorder.
 1678. The method of claim 1591 or 1592, wherein the health condition is a specific phobia.
 1679. The method of claim 1591 or 1592, wherein the health condition is agoraphobia.
 1680. The method of claim 1591 or 1592, wherein the health condition is social anxiety disorder.
 1681. The method of claim 1591 or 1592, wherein the health condition is separation anxiety disorder.
 1682. The method of claim 1591 or 1592, wherein the health condition is panic disorder.
 1683. The method of claim 1591 or 1592, wherein the health condition is selective mutism.
 1684. The method of claim 1591 or 1592, wherein the health condition is obsessive-compulsive disorder.
 1685. The method of claim 1591 or 1592, wherein the health condition is depression.
 1686. The method of claim 1591 or 1592, wherein the health condition is a major depressive disorder with psychotic feature(s).
 1687. The method of claim 1591 or 1592, wherein the health condition is psychotic depression.
 1688. The method of claim 1591 or 1592, wherein the health condition is paranoia.
 1689. The method of claim 1591 or 1592, wherein the health condition is psychosis.
 1690. The method of claim 1591 or 1592, wherein the health condition is early psychosis.
 1691. The method of claim 1591 or 1592, wherein the health condition is an unspecified psychosis.
 1692. The method of claim 1591 or 1592, wherein the health condition is an unspecified reactive psychosis.
 1693. The method of claim 1591 or 1592, wherein the health condition is a psychotic disorder.
 1694. The method of claim 1591 or 1592, wherein the health condition is a brief psychotic disorder.
 1695. The method of claim 1591 or 1592, wherein the health condition is a debilitating psychiatric disorder.
 1696. The method of claim 1591 or 1592, wherein the health condition is schizophrenia.
 1697. The method of claim 1591 or 1592, wherein the health condition is schizophreniform disorder.
 1698. The method of claim 1591 or 1592, wherein the health condition is schizoaffective disorder.
 1699. The method of claim 1591 or 1592, wherein the health condition is paranoid personality disorder.
 1700. The method of claim 1591 or 1592, wherein the health condition is schizoid personality disorder.
 1701. The method of claim 1591 or 1592, wherein the health condition is schizotypal personality disorder.
 1702. The method of claim 1591 or 1592, wherein the health condition is a shared psychotic disorder.
 1703. The method of claim 1591 or 1592, wherein the health condition is a shared paranoia disorder.
 1704. The method of claim 1591 or 1592, wherein the health condition is a delusional disorder.
 1705. The method of claim 1591 or 1592, wherein the health condition is bipolar disorder.
 1706. The method of claim 1591 or 1592, wherein the health condition is bipolar I disorder.
 1707. The method of claim 1591 or 1592, wherein the health condition is bipolar II disorder.
 1708. The method of claim 1591 or 1592, wherein the health condition is mania.
 1709. The method of claim 1591 or 1592, wherein the health condition is manic disorder.
 1710. The method of claim 1591 or 1592, wherein the health condition is manic-depressive psychosis.
 1711. The method of claim 1591 or 1592, wherein the health condition is an addiction.
 1712. The method of claim 1591 or 1592, wherein the health condition is an addiction to alcohol.
 1713. The method of claim 1591 or 1592, wherein the health condition is an addiction to tobacco.
 1714. The method of claim 1591 or 1592, wherein the health condition is an addiction to nicotine.
 1715. The method of claim 1591 or 1592, wherein the health condition is an addiction to an opiate.
 1716. The method of claim 1591 or 1592, wherein the health condition is an addiction to a stimulant.
 1717. The method of claim 1591 or 1592, wherein the health condition is an addiction to a prescription drug.
 1718. The method of claim 1591 or 1592, wherein the health condition is an addiction to gambling.
 1719. The method of claim 1591 or 1592, wherein the health condition is an addiction to food.
 1720. The method of claim 1591 or 1592, wherein the health condition is an addiction to shopping.
 1721. The method of claim 1591 or 1592, wherein the health condition is an addiction to the internet.
 1722. The method of claim 1591 or 1592, wherein the health condition is an addiction to sex.
 1723. The method of claim 1591 or 1592, wherein the health condition is drug withdrawal.
 1724. The method of claim 1591 or 1592, wherein the health condition is alcohol withdrawal syndrome.
 1725. The method of claim 1591 or 1592, wherein the health condition is nicotine withdrawal.
 1726. The method of claim 1591 or 1592, wherein the health condition is opioid withdrawal.
 1727. The method of claim 1591 or 1592, wherein the health condition is cannabis withdrawal.
 1728. The method of claim 1591 or 1592, wherein the health condition is benzodiazepine withdrawal syndrome.
 1729. The method of claim 1591 or 1592, wherein the health condition is antidepressant discontinuation syndrome.
 1730. The method of claim 1591 or 1592, wherein the health condition is antipsychotic withdrawal syndrome.
 1731. The method of claim 1591 or 1592, wherein the health condition is addictive behavior.
 1732. The method of claim 1591 or 1592, wherein the health condition is cannabis use disorder.
 1733. The method of claim 1591 or 1592, wherein the health condition is attention deficit hyperactivity disorder (“ADHD”).
 1734. The method of claim 1591 or 1592, wherein the health condition is autism or an autism spectrum disorder.
 1735. The method of claim 1591 or 1592, wherein the health condition is Asperger syndrome.
 1736. The method of claim 1591 or 1592, wherein the health condition is fragile X syndrome.
 1737. The method of claim 1591 or 1592, wherein the health condition is a pervasive developmental disorder not otherwise specified (“PDD-NOS”).
 1738. The method of claim 1591 or 1592, wherein the health condition is a childhood disintegrative disorder.
 1739. The method of claim 1591 or 1592, wherein the health condition is Tourette's syndrome.
 1740. The method of claim 1591 or 1592, wherein the health condition is Down syndrome.
 1741. The method of claim 1591 or 1592, wherein the health condition is post-traumatic stress disorder (“PTSD”).
 1742. The method of claim 1591 or 1592, wherein the health condition is asthma.
 1743. The method of claim 1591 or 1592, wherein the health condition is respiratory disease.
 1744. The method of claim 1591 or 1592, wherein the health condition is chronic lower respiratory disease.
 1745. The method of claim 1591 or 1592, wherein the health condition is chronic obstructive pulmonary disease (“COPD”).
 1746. The method of claim 1591 or 1592, wherein the health condition is insomnia.
 1747. The method of claim 1591 or 1592, wherein the health condition is sleep apnea.
 1748. The method of claim 1591 or 1592, wherein the health condition is obstructive sleep apnea.
 1749. The method of claim 1591 or 1592, wherein the health condition is or restless legs syndrome.
 1750. The method of claim 1591 or 1592, wherein the health condition is cramping.
 1751. The method of claim 1591 or 1592, wherein the health condition is muscle spasms.
 1752. The method of claim 1591 or 1592, wherein the health condition is spasticity.
 1753. The method of claim 1591 or 1592, wherein the health condition is spasmodic torticollis.
 1754. The method of claim 1591 or 1592, wherein the health condition is a dyskinetic movement disorder.
 1755. The method of claim 1591 or 1592, wherein the health condition is dystonia.
 1756. The method of claim 1591 or 1592, wherein the health condition is intractable spasticity.
 1757. The method of claim 1591 or 1592, wherein the health condition is intractable skeletal muscular spasticity.
 1758. The method of claim 1591 or 1592, wherein the health condition is inclusion body myositis.
 1759. The method of claim 1591 or 1592, wherein the health condition is myasthenia gravis.
 1760. The method of claim 1591 or 1592, wherein the health condition is muscular dystrophy.
 1761. The method of claim 1591 or 1592, wherein the health condition is Duchenne muscular dystrophy.
 1762. The method of claim 1591 or 1592, wherein the health condition is muscle tremor.
 1763. The method of claim 1591 or 1592, wherein the health condition is cerebellar tremor.
 1764. The method of claim 1591 or 1592, wherein the health condition is dystonic tremor.
 1765. The method of claim 1591 or 1592, wherein the health condition is essential tremor.
 1766. The method of claim 1591 or 1592, wherein the health condition is orthostatic tremor.
 1767. The method of claim 1591 or 1592, wherein the health condition is Parkinsonian tremor.
 1768. The method of claim 1591 or 1592, wherein the health condition is physiological tremor.
 1769. The method of claim 1591 or 1592, wherein the health condition is psychogenic tremor.
 1770. The method of claim 1591 or 1592, wherein the health condition is rubral tremor.
 1771. The method of claim 1591 or 1592, wherein the health condition is nystagmus.
 1772. The method of claim 1591 or 1592, wherein the health condition is a seizure disorder.
 1773. The method of claim 1591 or 1592, wherein the health condition is recurrent focal seizures.
 1774. The method of claim 1591 or 1592, wherein the health condition is recurrent generalized seizures.
 1775. The method of claim 1591 or 1592, wherein the health condition is recurrent absence seizures.
 1776. The method of claim 1591 or 1592, wherein the health condition is recurrent myoclonic-absence seizures.
 1777. The method of claim 1591 or 1592, wherein the health condition is recurrent myoclonus.
 1778. The method of claim 1591 or 1592, wherein the health condition is recurrent myoclonic seizures.
 1779. The method of claim 1591 or 1592, wherein the health condition is recurrent tonic seizures.
 1780. The method of claim 1591 or 1592, wherein the health condition is recurrent tonic-clonic seizures.
 1781. The method of claim 1591 or 1592, wherein the health condition is recurrent atonic seizures.
 1782. The method of claim 1591 or 1592, wherein the health condition is recurrent chronic seizures.
 1783. The method of claim 1591 or 1592, wherein the health condition is epilepsy.
 1784. The method of claim 1591 or 1592, wherein the health condition is recurrent epileptic spasms.
 1785. The method of claim 1591 or 1592, wherein the health condition is refractory epilepsy.
 1786. The method of claim 1591 or 1592, wherein the health condition is intractable epilepsy.
 1787. The method of claim 1591 or 1592, wherein the health condition is treatment-resistant epilepsy.
 1788. The method of claim 1591 or 1592, wherein the health condition is Lennox-Gastaut syndrome.
 1789. The method of claim 1591 or 1592, wherein the health condition is Dravet syndrome.
 1790. The method of claim 1591 or 1592, wherein the health condition is febrile infection related epilepsy syndrome (“FIRES”).
 1791. The method of claim 1591 or 1592, wherein the health condition is juvenile myoclonic epilepsy.
 1792. The method of claim 1591 or 1592, wherein the health condition is myoclonic absence seizures (“MAS”).
 1793. The method of claim 1591 or 1592, wherein the health condition is myoclonic astatic epilepsy (“MAE”).
 1794. The method of claim 1591 or 1592, wherein the health condition is tuberous sclerosis complex (“TSC”).
 1795. The method of claim 1591 or 1592, wherein the health condition is Rett syndrome.
 1796. The method of claim 1591 or 1592, wherein the health condition is Angelman syndrome.
 1797. The method of claim 1591 or 1592, wherein the health condition is a neurological condition.
 1798. The method of claim 1591 or 1592, wherein the health condition is stroke.
 1799. The method of claim 1591 or 1592, wherein the health condition is hemorrhagic stroke.
 1800. The method of claim 1591 or 1592, wherein the health condition is ischemic stroke.
 1801. The method of claim 1591 or 1592, wherein the health condition is neonatal hypoxic-ischemic encephalopathy (“NHIE”).
 1802. The method of claim 1591 or 1592, wherein the health condition is hydrocephalus.
 1803. The method of claim 1591 or 1592, wherein the health condition is hydromyelia.
 1804. The method of claim 1591 or 1592, wherein the health condition is traumatic brain injury (“TBI”).
 1805. The method of claim 1591 or 1592, wherein the health condition is post-concussion syndrome.
 1806. The method of claim 1591 or 1592, wherein the health condition is chronic traumatic encephalopathy.
 1807. The method of claim 1591 or 1592, wherein the health condition is a spinal cord injury.
 1808. The method of claim 1591 or 1592, wherein the health condition is a spinal cord disease.
 1809. The method of claim 1591 or 1592, wherein the health condition is syringomyelia.
 1810. The method of claim 1591 or 1592, wherein the health condition is Tarlov cysts.
 1811. The method of claim 1591 or 1592, wherein the health condition is cystic fibrosis.
 1812. The method of claim 1591 or 1592, wherein the health condition is cerebral palsy.
 1813. The method of claim 1591 or 1592, wherein the health condition is spinocerebellar ataxia.
 1814. The method of claim 1591 or 1592, wherein the health condition is a neural-tube defect.
 1815. The method of claim 1591 or 1592, wherein the health condition is neuropathy.
 1816. The method of claim 1591 or 1592, wherein the health condition is a brain tumor.
 1817. The method of claim 1591 or 1592, wherein the health condition is glioblastoma multiforme.
 1818. The method of claim 1591 or 1592, wherein the health condition is glioblastoma astrocytoma.
 1819. The method of claim 1591 or 1592, wherein the health condition is neurofibromatosis.
 1820. The method of claim 1591 or 1592, wherein the health condition is Arnold-Chiari malformation.
 1821. The method of claim 1591 or 1592, wherein the health condition is or multiple sclerosis.
 1822. The method of claim 1591 or 1592, wherein the health condition is a connective tissue disorder.
 1823. The method of claim 1591 or 1592, wherein the health condition is Ehlers-Danlos syndrome.
 1824. The method of claim 1591 or 1592, wherein the health condition is fibrous dysplasia.
 1825. The method of claim 1591 or 1592, wherein the health condition is osteogenesis imperfecta.
 1826. The method of claim 1591 or 1592, wherein the health condition is nail-patella syndrome.
 1827. The method of claim 1591 or 1592, wherein the health condition is idiopathic pulmonary fibrosis.
 1828. The method of claim 1591 or 1592, wherein the health condition is bone loss.
 1829. The method of claim 1591 or 1592, wherein the health condition is bone loss caused by a bone fracture.
 1830. The method of claim 1591 or 1592, wherein the health condition is bone loss caused by a surgical procedure.
 1831. The method of claim 1591 or 1592, wherein the health condition is a periodontal defect.
 1832. The method of claim 1591 or 1592, wherein the health condition is periodontal disease.
 1833. The method of claim 1591 or 1592, wherein the health condition is osteopenia.
 1834. The method of claim 1591 or 1592, wherein the health condition is an osteolytic bone disease.
 1835. The method of claim 1591 or 1592, wherein the health condition is osteoporosis.
 1836. The method of claim 1591 or 1592, wherein the health condition is age-related osteoporosis.
 1837. The method of claim 1591 or 1592, wherein the health condition is hormone-related osteoporosis.
 1838. The method of claim 1591 or 1592, wherein the health condition is hypogonadism-related osteoporosis.
 1839. The method of claim 1591 or 1592, wherein the health condition is diabetes-related osteoporosis.
 1840. The method of claim 1591 or 1592, wherein the health condition is glucocorticoid-related osteoporosis.
 1841. The method of claim 1591 or 1592, wherein the health condition is or disuse osteoporosis.
 1842. The method of claim 1591 or 1592, wherein the health condition is a carcinoma.
 1843. The method of claim 1591 or 1592, wherein the health condition is sarcoma.
 1844. The method of claim 1591 or 1592, wherein the health condition is lymphoma.
 1845. The method of claim 1591 or 1592, wherein the health condition is leukemia.
 1846. The method of claim 1591 or 1592, wherein the health condition is germ cell tumor.
 1847. The method of claim 1591 or 1592, wherein the health condition is or blastoma.
 1848. The method of claim 1591 or 1592, wherein the health condition is condition is brain cancer.
 1849. The method of claim 1591 or 1592, wherein the health condition is ovarian cancer.
 1850. The method of claim 1591 or 1592, wherein the health condition is breast cancer.
 1851. The method of claim 1591 or 1592, wherein the health condition is vaginal cancer.
 1852. The method of claim 1591 or 1592, wherein the health condition is vulvar cancer.
 1853. The method of claim 1591 or 1592, wherein the health condition is uterine cancer.
 1854. The method of claim 1591 or 1592, wherein the health condition is cervical cancer.
 1855. The method of claim 1591 or 1592, wherein the health condition is endometrial cancer.
 1856. The method of claim 1591 or 1592, wherein the health condition is prostate cancer.
 1857. The method of claim 1591 or 1592, wherein the health condition is testicular cancer.
 1858. The method of claim 1591 or 1592, wherein the health condition is penile cancer.
 1859. The method of claim 1591 or 1592, wherein the health condition is liver cancer.
 1860. The method of claim 1591 or 1592, wherein the health condition is intrahepatic bile duct cancer.
 1861. The method of claim 1591 or 1592, wherein the health condition is lung cancer.
 1862. The method of claim 1591 or 1592, wherein the health condition is small cell lung cancer.
 1863. The method of claim 1591 or 1592, wherein the health condition is non-small cell lung cancer.
 1864. The method of claim 1591 or 1592, wherein the health condition is bronchial cancer.
 1865. The method of claim 1591 or 1592, wherein the health condition is mesothelioma.
 1866. The method of claim 1591 or 1592, wherein the health condition is pancreatic cancer.
 1867. The method of claim 1591 or 1592, wherein the health condition is gall bladder cancer.
 1868. The method of claim 1591 or 1592, wherein the health condition is non-melanoma skin cancer.
 1869. The method of claim 1591 or 1592, wherein the health condition is melanoma.
 1870. The method of claim 1591 or 1592, wherein the health condition is Kaposi sarcoma.
 1871. The method of claim 1591 or 1592, wherein the health condition is thyroid cancer.
 1872. The method of claim 1591 or 1592, wherein the health condition is head and neck cancer.
 1873. The method of claim 1591 or 1592, wherein the health condition is nasopharyngeal cancer.
 1874. The method of claim 1591 or 1592, wherein the health condition is oropharyngeal cancer.
 1875. The method of claim 1591 or 1592, wherein the health condition is hypopharyngeal cancer.
 1876. The method of claim 1591 or 1592, wherein the health condition is laryngeal cancer.
 1877. The method of claim 1591 or 1592, wherein the health condition is oral cavity cancer.
 1878. The method of claim 1591 or 1592, wherein the health condition is tongue cancer.
 1879. The method of claim 1591 or 1592, wherein the health condition is mouth cancer.
 1880. The method of claim 1591 or 1592, wherein the health condition is salivary gland cancer.
 1881. The method of claim 1591 or 1592, wherein the health condition is esophageal cancer.
 1882. The method of claim 1591 or 1592, wherein the health condition is gastric cancer.
 1883. The method of claim 1591 or 1592, wherein the health condition is colorectal cancer.
 1884. The method of claim 1591 or 1592, wherein the health condition is colon cancer.
 1885. The method of claim 1591 or 1592, wherein the health condition is rectal cancer.
 1886. The method of claim 1591 or 1592, wherein the health condition is anal cancer.
 1887. The method of claim 1591 or 1592, wherein the health condition is kidney cancer.
 1888. The method of claim 1591 or 1592, wherein the health condition is renal cell cancer.
 1889. The method of claim 1591 or 1592, wherein the health condition is renal pelvis cancer.
 1890. The method of claim 1591 or 1592, wherein the health condition is bladder cancer.
 1891. The method of claim 1591 or 1592, wherein the health condition is urethral cancer.
 1892. The method of claim 1591 or 1592, wherein the health condition is Hodgkin lymphoma.
 1893. The method of claim 1591 or 1592, wherein the health condition is non-Hodgkin's lymphoma.
 1894. The method of claim 1591 or 1592, wherein the health condition is myeloma.
 1895. The method of claim 1591 or 1592, wherein the health condition is multiple myeloma.
 1896. The method of claim 1591 or 1592, wherein the health condition is acute lymphocytic leukemia.
 1897. The method of claim 1591 or 1592, wherein the health condition is chronic lymphocytic leukemia.
 1898. The method of claim 1591 or 1592, wherein the health condition is acute myeloid leukemia.
 1899. The method of claim 1591 or 1592, wherein the health condition is chronic myeloid leukemia.
 1900. The method of claim 1591 or 1592, wherein the health condition is osteosarcoma.
 1901. The method of claim 1591 or 1592, wherein the health condition is soft tissue cancer.
 1902. The method of any one of claims 1591-1901, wherein at least one symptom of the health condition is pain; and the composition is administered to treat pain.
 1903. The method of any one of claims 1591-1901, wherein at least one symptom of the health condition is inflammation; and the composition is administered to treat inflammation.
 1904. The method of any one of claims 1591-1901, wherein at least one symptom of the health condition is anxiety; and the composition is administered to treat anxiety.
 1905. The method of any one of claims 1591-1901, wherein the subject presents with both the health condition and hypertension; hypertension exacerbates the health condition; and the composition is administered to treat the hypertension.
 1906. The method of any one of claims 1591-1901, wherein the subject presents with both the health condition and pre-hypertension; either pre-hypertension or hypertension exacerbates the health condition; and the composition is administered to either treat the pre-hypertension or reduce the risk that the subject will develop hypertension.
 1907. The method of any one of claims 1591-1901, wherein diuretic properties of the cannabinoid anion treat the health condition.
 1908. The method of any one of claims 1591-1901, wherein the health condition is an autoimmune disease; and the composition is administered to inhibit aberrant immune response in the subject.
 1909. The method of any one of claims 1591-1901, wherein aberrant tumor necrosis factor alpha (“TNF-alpha”) signaling either causes or exacerbates the health condition; and the composition is administered to inhibit TNF-alpha-mediated signaling pathways.
 1910. The method of any one of claims 1591-1901, wherein aberrant interferon gamma (“INF-gamma”) signaling either causes or exacerbates the health condition; and the composition is administered to inhibit INF-gamma-mediated signaling pathways.
 1911. The method of any one of claims 1591-1901, wherein at least one symptom of the health condition is muscle cramping, spasticity, tremor, or muscle spasms; and the composition is administered to treat the muscle cramping, spasticity, tremor, or muscle spasms.
 1912. The method of any one of claims 1591-1901, wherein at least one symptom of the health condition is seizures; and the composition is administered to treat seizures.
 1913. The method of any one of claims 1591-1901, wherein at least one symptom of the health condition is appetite suppression, nausea, or vomiting; and the composition is administered to treat the appetite suppression, nausea, or vomiting.
 1914. The method of any one of claims 1591-1901, wherein the subject is receiving a primary pharmaceutical agent to treat the health condition; the primary pharmaceutical agent causes appetite suppression, nausea, or vomiting; and the composition is administered to treat the appetite suppression, nausea, or vomiting.
 1915. The method of any one of claims 1591-1901, wherein at least one symptom of the health condition is decreased bone density; and the composition is administered to treat bone loss.
 1916. The method of any one of claims 1591-1901, wherein the health condition is a terminal illness; and the composition is administered to provide palliative care. 